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  1. Article: The Tomographic Study and the Phenotype of Wormian Bones.

    Al Kaissi, Ali / Ryabykh, Sergey / Ben Chehida, Farid / Al Kaissi, Hamza / Kircher, Susanne Gerit / Stransky, Martin J / Grill, Franz

    Diagnostics (Basel, Switzerland)

    2023  Volume 13, Issue 5

    Abstract: Background: We describe patients who were recognized via conventional radiographs of the skull as manifesting wormian bones. Wormian bones are not a specific diagnostic entity and can be seen in variable forms of syndromic disorders.: Materials and ... ...

    Abstract Background: We describe patients who were recognized via conventional radiographs of the skull as manifesting wormian bones. Wormian bones are not a specific diagnostic entity and can be seen in variable forms of syndromic disorders.
    Materials and methods: Seven children and three adults (of 10-28 years) were seen and diagnosed in our departments. The principal complaints for the pediatric and adult group were: ligamentous hyperlaxity, a history of delayed walking and occasional fractures, which later in life started to manifest a constellation of neurological symptoms such as nystagmus, persistent headache, and apnea. Conventional radiographs were the first traditional tools used to recognize wormian bones. We performed 3D reconstruction CT scans to further understand the precise etiology and the nature of these wormian bones and attempted to connect them with a broad spectrum of unpleasant clinical presentations. Our group of patients was consistent with the phenotypic and genotypic diagnoses of osteogenesis imperfecta type I and type IV as well as patients with multicentric
    Results: Three-dimensional reconstruction CT scan of the skulls confirmed that these worm-like phenotypes are in fact stemmed from the progressive softening of the sutures. The overall phenotype of the melted sutures is akin to overly stretched pastry. The most concerning sutures in this pathological process are the lambdoid. The overstretching of the lambdoid sutures was responsible for the development of sub-clinical basilar impression/invagination. Patients with certain forms of skeletal dysplasia such as osteogenesis imperfecta type I and
    Conclusion: What we encountered via 3D reconstruction CT scan in our group of patients was entirely different than the traditional description that can be found in all relevant literature of the last decades. The worm-like phenomenon is in fact a pathological sequel occurring as a result of a progressive softening of the sutures, which results in the overstretching of the lambdoid sutures, a pathological process roughly similar to an overly stretched soft pastry. This softening is totally connected to the weight of the cerebrum (the occipital lobe of the cerebrum). The lambdoid sutures represent the weight-bearing zone of the skull. When these joints are loose and soft, they adversely alter the anatomical structures of the skull and lead to a highly hazardous derangement of the craniocervical junction. The latter causes the pathological upward invasion of the dens into the brain stem, leading to the development of morbid/mortal basilar impression/invagination.
    Language English
    Publishing date 2023-02-24
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662336-5
    ISSN 2075-4418
    ISSN 2075-4418
    DOI 10.3390/diagnostics13050874
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia.

    Al Kaissi, Ali / Ryabykh, Sergey / Kenis, Vladimir / Ben Chehida, Farid / Al Kaissi, Hamza / Kircher, Susanne Gerit / Grill, Franz

    Children (Basel, Switzerland)

    2023  Volume 10, Issue 10

    Abstract: Background: The diagnostic process for children and adults manifesting a constellation of ectodermal abnormalities requires a conscientious and highly structured process.: Material and methods: Six girls (aged 6-month-8 years) and two older girls ( ... ...

    Abstract Background: The diagnostic process for children and adults manifesting a constellation of ectodermal abnormalities requires a conscientious and highly structured process.
    Material and methods: Six girls (aged 6-month-8 years) and two older girls (aged 13 and 16 years) were born with variable skin lesions of varying intensities associated with noticeable cranial and skeletal malformation complexes. Cleft palate, abnormal dentition, and multiple papillomas were evident around the mouth, mostly bilateral but asymmetrical in the upper and lower limbs. Exaggerated frontal bossing (macrocephaly) and in some patients' microcephaly with variable skeletal defects of the craniocervical junction and diverse forms of lower limb deformities of syndactyly, polydactyly, and split-hand/foot (ectrodactyly).
    Results: All patients manifested the constellation of abnormalities with variable intensities ranging between alopecia, papillomas, striated skin pigmentations split-hand/foot (ectrodactyly), and major bone defects. A 3D reconstruction CT scan was directed mainly to further scrutinize children with pseudo cleft lip, submucus cleft, and cleft palate. Interstingly, they manifested massive demineralization of the cranium associated with severely defective dentition. A spine 3D reconstruction CT scan in two girls showed marked cystic cavitation of the upper jaw associated with excessive cavitation of the mastoid, causing tremendous frailty of the mastoid bone. A 3D sagittal CT scan showed odontoid hypoplasia and C1-2 instability associated with the rudimentary atlas and the persistence of extensive synchondrosis of the cervico-thoracic spine. The overall clinical and radiological phenotypic characterizations were consistent with the diagnosis of focal dermal hypoplasia (Goltz syndrome). Two children manifested heterozygous mutations in the PORCN gene, chromosome Xp11.
    Conclusions: In this study, we believe it's a good opportunity to share our novel scientific findings, which are intriguing and can be inspiring to readers, and to further aid the current scientific literature with exceptionally new unveiling results. This is the first comprehensive study of the cranio-skeletal malformation complex in children with GS.
    Language English
    Publishing date 2023-10-22
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2732685-8
    ISSN 2227-9067
    ISSN 2227-9067
    DOI 10.3390/children10101715
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives.

    Al Kaissi, Ali / Ryabykh, Sergey / Chehida, Farid Ben / Al Kaissi, Hamza / Kircher, Susanne Gerit / Grill, Franz / Guben, Alexander

    Children (Basel, Switzerland)

    2023  Volume 10, Issue 7

    Abstract: Background: Omitting the early closure of the cranial sutures in newly born children is not an uncommon practice. We describe the natural history of several unrelated children and adults from two unrelated families. These children were born with ... ...

    Abstract Background: Omitting the early closure of the cranial sutures in newly born children is not an uncommon practice. We describe the natural history of several unrelated children and adults from two unrelated families. These children were born with variable clinical manifestations: craniofacial asymmetry, ocular proptosis, floppiness, and progressive deceleration in cognitive development. None of these children underwent a cranial sutures assessment. False diagnoses of positional plagiocephaly, neonatal thyrotoxicosis, congenital muscular atrophy, and hydrocephalus were given to the parents. This sort of malpractice was the reason behind a sequence of devastating pathological events that occurred in the lifetime of these children and adults.
    Material and methods: This was a multigenerational study of two unrelated families. In total, we studied three children (aged 7-19 years) and three adults (aged 40-52 years) from two families. The children from the first family were referred to our departments because of pre-pubertal scoliosis, kyphoscoliosis, and early-onset osteoarthritis. Reading the clinical histories of these children signified apparent clinical misconceptions. For instance, craniofacial asymmetry was misinterpreted as positional plagiocephaly and treated by means of helmet molding therapy. Ocular proptosis was given the false diagnosis of neonatal thyrotoxicosis. Floppiness (hypotonia) was misdiagnosed as congenital muscular dystrophy. The index case from the second family showed progressive deceleration in his cognitive development, associated with signs of increased intracranial pressure. The only diagnosis was Dandy-Walker malformation. We documented every patient in accordance with the clinical and radiological phenotypic characterizations. The genotype characterization followed accordingly.
    Results: All patients in family (I) manifested a phenotype consistent to a certain extent with the clinical phenotype of Shprintzen-Goldberg syndrome (SGS), though the intensity of spine deformities was greater than has been described in the literature. The second family showed a constellation of Marfanoid habitus, craniosynostosis, increased intracranial pressure, hydrocephalus, Dandy-Walker malformation, seizures, and intellectual disability. The overall clinical phenotype was consistent but not fully diagnostic of craniosynostosis-Dandy-Walker-malformation hydrocephalus syndrome. The early closure of the sutures was totally different from one patient to another, including the premature closure of the metopic, coronal, squamosal, and sagittal sutures. One patient from family (II) underwent the implementation of a shunt system at the age of 3 years, unfortunately passing over the pre-existing craniosynostosis. In addition to skeletal deformities, a history of seizures and severe intellectual disability was recorded. The proband underwent chromosomal karyotyping, the FISH test, and whole-exome sequencing.
    Conclusion: The purpose of this study was fivefold. Firstly, to gain a meticulous understanding in order to differentiate between positional plagiocephaly, hypotonia, and congenital exophthalmos and their connections to abnormal craniofacial contours was and still is our first and foremost concern. Secondly, we aimed to characterize craniosynostosis, seizures, intellectual disabilities, and hydrocephalus associated with Marfanoid habitus, which were clearly demonstrated in our patients. Thirdly, we aimed to address the imperative for interpretations of clinical and radiological phenotypes and relate these tools to etiological understanding, which is an essential basis for diagnosis in the majority of long-term pediatric admissions. Fourthly, we aimed to assess the impacts of the missed early closure by the pediatricians and pediatric neurologists, which added a heavy pathological burden on these patients and their families. Fifthly, we aimed to identify whether early and diligent recognition can assist in cranial vault remodeling via surgical intervention to halt premature cranial suture fusions and can possibly alter the devastating course and the complications of the synostosed sutures.
    Language English
    Publishing date 2023-07-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2732685-8
    ISSN 2227-9067
    ISSN 2227-9067
    DOI 10.3390/children10071240
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Comparison of fruit characteristics, oil properties and fatty acid composition of local Syrian Kaissy cv olive (Olea europaea)

    Al-Bachir, M

    Journal of food measurement & characterization. 2017 Sept., v. 11, no. 3

    2017  

    Abstract: Characterization of Syrian (Kaissy cultivar) olive fruits and evaluation of physic-chemical ... of chemical properties of Syrian Kaissy cultivar olive oils (SKOO) including acid value, peroxide vale, Thiobarbituric ... for 3 years production of Syrian Kaissy cultivar olive fruit and oil are discussed in detail. ...

    Abstract Characterization of Syrian (Kaissy cultivar) olive fruits and evaluation of physic-chemical properties of oils were carried out during 3 years of production. The mean values of data for both measured and calculated variables of fruits were: grain length (21.89 mm), grain width (17.92 mm), length/width (1.22), weight of grain (3.79 g), weight of pulp (flesh) (3.19 g), weight of pit (0.60 g), pulp/pit ratio (5.35), crude oil (17.13%), water content (moisture) (51.34%). The 3 year average values of chemical properties of Syrian Kaissy cultivar olive oils (SKOO) including acid value, peroxide vale, Thiobarbituric acid value, iodine value(IV), saponification value, and phenolic content were 0.58%, 4.33 mEq O₂ kg⁻ ¹, 0.028 mg MDA kg⁻ ¹ oil, 90.77 g I₂, 100 g⁻ ¹, 194.91 mg KOH g⁻ ¹, and 218.08 g gallic acid kg⁻ ¹, respectively. Pefractive index (RI), and viscosity were 1.4666 nD at 25 °C and 139.56 mPa.s, respectively. However, the 2 years average values of Hunter’s color parameters of SKOO were; the lightness (L*= 66.91), redness (a* = 18.80), yellowness (b* = 29.08) and the color differences (∆E = 65.49). FA analysis of the SKOO used showed a high content of monounsaturated fatty acids (oleic acid 70.82% and palmitic acid 1.01%) and low polyunsaturated fatty acids (Linoleic acid 10.72% and Linolenic 0.82%) and saturated fatty acids (Palmitic 14.10% and stearic 2.57%). Results for 3 years production of Syrian Kaissy cultivar olive fruit and oil are discussed in detail.
    Keywords Olea europaea ; acid value ; color ; cultivars ; fruits ; gallic acid ; iodine ; iodine value ; linoleic acid ; oleic acid ; olive oil ; olives ; oxygen ; palmitic acid ; physicochemical properties ; polyunsaturated fatty acids ; potassium hydroxide ; pulp ; saponification ; viscosity ; water content
    Language English
    Dates of publication 2017-09
    Size p. 1011-1018.
    Publishing place Springer US
    Document type Article
    ZDB-ID 2754612-3
    ISSN 2193-4134 ; 2193-4126
    ISSN (online) 2193-4134
    ISSN 2193-4126
    DOI 10.1007/s11694-017-9476-7
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: The Tomographic Study and the Phenotype of Wormian Bones

    Ali Al Kaissi / Sergey Ryabykh / Farid Ben Chehida / Hamza Al Kaissi / Susanne Gerit Kircher / Martin J. Stransky / Franz Grill

    Diagnostics, Vol 13, Iss 874, p

    2023  Volume 874

    Abstract: Background: We describe patients who were recognized via conventional radiographs of the skull as manifesting wormian bones. Wormian bones are not a specific diagnostic entity and can be seen in variable forms of syndromic disorders. Materials and ... ...

    Abstract Background: We describe patients who were recognized via conventional radiographs of the skull as manifesting wormian bones. Wormian bones are not a specific diagnostic entity and can be seen in variable forms of syndromic disorders. Materials and Methods: Seven children and three adults (of 10–28 years) were seen and diagnosed in our departments. The principal complaints for the pediatric and adult group were: ligamentous hyperlaxity, a history of delayed walking and occasional fractures, which later in life started to manifest a constellation of neurological symptoms such as nystagmus, persistent headache, and apnea. Conventional radiographs were the first traditional tools used to recognize wormian bones. We performed 3D reconstruction CT scans to further understand the precise etiology and the nature of these wormian bones and attempted to connect them with a broad spectrum of unpleasant clinical presentations. Our group of patients was consistent with the phenotypic and genotypic diagnoses of osteogenesis imperfecta type I and type IV as well as patients with multicentric carpotarsal osteolysis syndrome. Results: Three-dimensional reconstruction CT scan of the skulls confirmed that these worm-like phenotypes are in fact stemmed from the progressive softening of the sutures. The overall phenotype of the melted sutures is akin to overly stretched pastry. The most concerning sutures in this pathological process are the lambdoid. The overstretching of the lambdoid sutures was responsible for the development of sub-clinical basilar impression/invagination. Patients with certain forms of skeletal dysplasia such as osteogenesis imperfecta type I and IV manifested the heterozygous mutation of COL1A1/COLA2, shown as typical overstretching of the sutures . Similarly, patients with multicentric carpotarsal osteolysis syndrome with a heterozygous missense mutation of MAFB also manifested the phenotype of overly stretched pastry along the skull sutures . Conclusion: What we encountered via 3D reconstruction CT scan in ...
    Keywords wormian bones ; radiology ; tomography ; phenotype ; overly stretched pastry ; bulging of the occipital lobe of the cerebrum ; Medicine (General) ; R5-920
    Subject code 610
    Language English
    Publishing date 2023-02-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Classic Cystic Fibrosis Presentation in Two Middle Eastern Siblings with a rare CFTR mutation (c.80G>T).

    Hafiz, Sumaiya / Al Qassimi, Sarah / Isse, Said / Wahla, Ali Saeed / El-Kaissi, Mahmoud / Uzbeck, Mateen / Shafiq, Irfan

    European journal of case reports in internal medicine

    2023  Volume 10, Issue 1, Page(s) 3728

    Abstract: Cystic fibrosis (CF) is a common autosomal recessive disorder which is mainly found in Caucasians but has also been reported in Asian populations. CF is primarily caused by mutations in the CFTR gene which regulates the transport of chloride ions across ... ...

    Abstract Cystic fibrosis (CF) is a common autosomal recessive disorder which is mainly found in Caucasians but has also been reported in Asian populations. CF is primarily caused by mutations in the CFTR gene which regulates the transport of chloride ions across the cell membrane. We describe the cases of two siblings with CF diagnosed with the rare missense mutation c.80G>T, which has only been referenced once in the literature and shows a possible association with classical form of CF.
    Learning points: c.80G>T is a very rare CFTR missense mutation which has not been known to be a disease-causing alteration.The mutation causes an amino acid switch from glycine to valine at position 27 in exon 2, resulting in the production of defective CFTR protein.In the homozygous state, c.80G>T seems to be associated with the classic CF phenotype.
    Language English
    Publishing date 2023-01-17
    Publishing country Italy
    Document type Journal Article
    ISSN 2284-2594
    ISSN (online) 2284-2594
    DOI 10.12890/2023_003728
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Classic Cystic Fibrosis Presentation in Two Middle Eastern Siblings with a rare CFTR mutation (c.80G>T)

    Sumaiya Hafiz / Sarah Al Qassimi / Ali Saeed Wahla / Mahmoud El-Kaissi / Mateen Uzbek / Irfan Shafiq

    European Journal of Case Reports in Internal Medicine (2023)

    2023  

    Abstract: Cystic fibrosis (CF) is a common autosomal recessive disorder which is mainly found in Caucasians but has also been reported in Asian populations. CF is primarily caused by mutations in the CFTR gene which regulates the transport of chloride ions across ... ...

    Abstract Cystic fibrosis (CF) is a common autosomal recessive disorder which is mainly found in Caucasians but has also been reported in Asian populations. CF is primarily caused by mutations in the CFTR gene which regulates the transport of chloride ions across the cell membrane. We describe the cases of two siblings with CF diagnosed with the rare missense mutation c.80G>T, which has only been referenced once in the literature and shows a possible association with classical form of CF.
    Keywords cystic fibrosis ; middle east ; cftr mutation ; c.80g>t ; Medicine ; R
    Language English
    Publishing date 2023-02-01T00:00:00Z
    Publisher SMC MEDIA SRL
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article: Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities.

    Al Kaissi, Ali / Ryabykh, Sergey / Nassib, Nabil / Bouchoucha, Sami / Benjemaa, Lamia / Rejeb, Imen / Hizem, Syrine / Kenis, Vladimir / Grill, Franz / Kircher, Susanne Gerit / Shboul, Mohammad / Ben Chehida, Farid

    Diagnostics (Basel, Switzerland)

    2022  Volume 12, Issue 10

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2022-09-30
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662336-5
    ISSN 2075-4418
    ISSN 2075-4418
    DOI 10.3390/diagnostics12102375
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  9. Article: Torticollis in Connection with Spine Phenotype.

    Al Kaissi, Ali / Nassib, Nabil / Bouchoucha, Sami / Shboul, Mohammad / Grill, Franz / Kircher, Susanne Gerit / Ochirova, Polina / Ryabykh, Sergey

    Diagnostics (Basel, Switzerland)

    2022  Volume 12, Issue 7

    Abstract: Purpose: Torticollis is not of uncommon occurrence in orthopaedic departments. Various theories and studies concerning the pathogenesis of the deformity have been suggested. We aimed to highlight and discuss the underlying cervical and spine ... ...

    Abstract Purpose: Torticollis is not of uncommon occurrence in orthopaedic departments. Various theories and studies concerning the pathogenesis of the deformity have been suggested. We aimed to highlight and discuss the underlying cervical and spine malformation complex in correlation with torticollis via radiographic and tomographic analysis and its connection with a specific syndromic entity.
    Methods: Torticollis has been recognised in six patients (2 boys and 4 girls with an age range of 14-18 years), in addition to a couple of parents manifested persistent backpain. A variable spine malformation complex was the main reason behind torticollis. In addition, some patients manifested plagiocephaly, facial asymmetry and scoliosis/kyphoscoliosis. In some patients, conventional radiographs were of limited value because of the overlapping anatomical structures. Three-dimensional reconstruction CT scanning was the modality of choice, which enlightens the path for the phenotypic characterisation.
    Results: A 16-year-old-boy presented with torticollis in correlation with pathologic aberration of the spine cartilaginous stage was analysed via 3DCT scan. Comprehensive clinical and radiological phenotypes were in favour of spondylomegepiphyseal dysplasia. The genotype showed a mutation of the NKX3-2 (BAPX1) gene compatible with the diagnosis of spondylo-meg-epiphyseal-metaphyseal dysplasia. His younger male sibling and parents were heterozygous carriers. In two patients with pseudoachondroplasia syndrome, in which odontoid hypoplasia associated with cervical spine synchondrosis causing life-threatening torticollis, Cartilage oligomeric matrix protein (COMP) gene mutation was identified. MURCS syndrome has been diagnosed in two unrelated girls. Torticollis associated with cervical kyphosis was the major presentation since early childhood. Interestingly, one girl showed omovertebral bones of the lower cervical and upper thoracic spine. Her karyotype manifested a balanced translocation of 46 XX, t (14q; 15q).
    Conclusion: To detect the underlying etiological diagnosis of torticollis, a skeletal survey was the primary diagnostic tool. Conventional radiographs of the craniocervical junction and spine resulted in confusing readings because of the overlapping anatomical structures. Cranio-cervical malformation complex could have serious neurological deficits, especially for children with indefinite diagnosis of torticollis. The widely used term of congenital muscular torticollis resulted in morbid or mortal consequences. Moreover, some patients received vigorous physical therapy on the bases of muscular torticollis. Sadly speaking, this resulted in grave complications. Understanding the imaging phenotype and the genotype in such patients is the baseline tool for precise and proper management. The value of this paper is to sensitise physicians and orthopaedic surgeons to the necessity of comprehensive clinical and radiological phenotypic characterisations in patients with long term skeletal pathology.
    Language English
    Publishing date 2022-07-09
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662336-5
    ISSN 2075-4418
    ISSN 2075-4418
    DOI 10.3390/diagnostics12071672
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan.

    Al Kaissi, Ali / Shboul, Mohammad / Kenis, Vladimir / Grill, Franz / Ganger, Rudolf / Kircher, Susanne Gerit

    Medicines (Basel, Switzerland)

    2019  Volume 6, Issue 2

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2019-05-29
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2777965-8
    ISSN 2305-6320
    ISSN 2305-6320
    DOI 10.3390/medicines6020060
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