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  1. Article ; Online: Homozygous

    Shajil, Chandana / Sathishkumar, Dharshini / Kumar, Sathish / Danda, Sumita

    BMJ case reports

    2024  Volume 17, Issue 1

    Abstract: A wide range of inherited and acquired conditions can manifest as infantile erythroderma, among ... ...

    Abstract A wide range of inherited and acquired conditions can manifest as infantile erythroderma, among which
    MeSH term(s) Infant ; Male ; Child ; Humans ; Dermatitis, Exfoliative/diagnosis ; Dermatitis, Exfoliative/genetics ; Acitretin ; Cyclosporine ; Guanylate Cyclase ; Membrane Proteins ; CARD Signaling Adaptor Proteins
    Chemical Substances Acitretin (LCH760E9T7) ; Cyclosporine (83HN0GTJ6D) ; CARD14 protein, human (EC 4.6.1.-) ; Guanylate Cyclase (EC 4.6.1.2) ; Membrane Proteins ; CARD Signaling Adaptor Proteins
    Language English
    Publishing date 2024-01-16
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1757-790X
    ISSN (online) 1757-790X
    DOI 10.1136/bcr-2022-254090
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Restrictive Dermopathy Due to

    Chiramel, Minu Jose / Sathishkumar, Dharshini / Santhanam, Sridhar / Ponmudi, Nithya J / Telugu, Ramesh Babu / Mohan, Sony / Athiyarath, Rekha

    Indian journal of dermatology

    2024  Volume 69, Issue 1, Page(s) 95–97

    Language English
    Publishing date 2024-02-27
    Publishing country India
    Document type Journal Article
    ZDB-ID 416069-1
    ISSN 1998-3611 ; 0019-5154
    ISSN (online) 1998-3611
    ISSN 0019-5154
    DOI 10.4103/ijd.ijd_681_23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.B 817: Show issues Location:
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  3. Article ; Online: Folliculocystic and Collagenous Hamartoma: A Rare Cutaneous Manifestation of Tuberous Sclerosis.

    Shajil, Chandana / Sathishkumar, Dharshini / Baitule, Amey / Chandy, Sujith

    Indian journal of dermatology

    2022  Volume 67, Issue 3, Page(s) 317

    Language English
    Publishing date 2022-10-28
    Publishing country India
    Document type Journal Article
    ZDB-ID 416069-1
    ISSN 1998-3611 ; 0019-5154
    ISSN (online) 1998-3611
    ISSN 0019-5154
    DOI 10.4103/ijd.ijd_88_22
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Algorithmic approach toward diagnosis of patients with congenital photosensitivity disorders and review of literature.

    Patro, Nibedita / Sathishkumar, Dharshini / Panda, Maitreyee / Mahajan, Rahul

    International journal of dermatology

    2023  Volume 63, Issue 3, Page(s) 298–305

    Abstract: The congenital photosensitivity disorders present as cutaneous signs and symptoms secondary to photosensitivity, extracutaneous manifestations, and a predisposition to malignancy. Diagnosis of these conditions mainly depend on clinical findings as the ... ...

    Abstract The congenital photosensitivity disorders present as cutaneous signs and symptoms secondary to photosensitivity, extracutaneous manifestations, and a predisposition to malignancy. Diagnosis of these conditions mainly depend on clinical findings as the molecular analysis is not always feasible. A review of all the related articles collected after a thorough literature search using keywords, "congenital AND photosensitivity NOT acquired" and the individual diseases was done. A total of 264 articles were included in the review. An algorithm for diagnosis of the different congenital photosensitivity disorders based on the various clinical presentations has been proposed. An early suspicion and diagnosis of the different congenital photosensitivity disorders is the cornerstone behind prompt institution of prevention and treatment, and decreasing the associated morbidity.
    MeSH term(s) Humans ; Photosensitivity Disorders/diagnosis ; Photosensitivity Disorders/etiology ; Photosensitivity Disorders/therapy ; Skin ; Algorithms
    Language English
    Publishing date 2023-12-19
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 412254-9
    ISSN 1365-4632 ; 0011-9059 ; 1461-1244
    ISSN (online) 1365-4632
    ISSN 0011-9059 ; 1461-1244
    DOI 10.1111/ijd.16965
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  5. Article ; Online: Spontaneous crateriform indentation in a child.

    Shajil, Chandana / Sathishkumar, Dharshini / Babu, Jyoti Sureka / Babu, Ramesh / Kumar, Sathish

    Pediatric dermatology

    2023  Volume 40, Issue 4, Page(s) 715–717

    MeSH term(s) Humans ; Child ; Skin ; Scleroderma, Localized ; Panniculitis
    Language English
    Publishing date 2023-07-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605539-4
    ISSN 1525-1470 ; 0736-8046
    ISSN (online) 1525-1470
    ISSN 0736-8046
    DOI 10.1111/pde.15241
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    Zs.A 1882: Show issues Location:
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  6. Article ; Online: Rapid recovery in a child with febrile ulceronecrotic Mucha-Habermann disease following intravenous immunoglobulin administration.

    Somasundaram, Arun / Gupta, Ankan / Sathishkumar, Dharshini / Mathew, Lydia / George, Anju / Thomas, Meera

    Pediatric dermatology

    2024  

    Abstract: Febrile ulceronecrotic Mucha-Habermann disease (FUMHD), a lymphocyte-mediated inflammatory skin disorder, is considered a severe variant of pityriasis lichenoides et varioliformis acuta that can lead to a fatal outcome if not managed in a timely fashion. ...

    Abstract Febrile ulceronecrotic Mucha-Habermann disease (FUMHD), a lymphocyte-mediated inflammatory skin disorder, is considered a severe variant of pityriasis lichenoides et varioliformis acuta that can lead to a fatal outcome if not managed in a timely fashion. Children with FUMHD can have systemic complications involving various organs. The scarcity of reported cases and the absence of well-designed studies or randomized clinical trials to evaluate different therapeutic modalities pose a major challenge in treating this potentially life-threatening disorder. We report a five-year-old child with FUMHD and seizures treated unsuccessfully with a combination of systemic steroids, methotrexate, dapsone, and oral erythromycin, who improved rapidly and achieved disease control with just a single infusion of low-dose intravenous immunoglobulin.
    Language English
    Publishing date 2024-01-17
    Publishing country United States
    Document type Case Reports
    ZDB-ID 605539-4
    ISSN 1525-1470 ; 0736-8046
    ISSN (online) 1525-1470
    ISSN 0736-8046
    DOI 10.1111/pde.15516
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  7. Article: A Puzzling Periumbilical Pigmented Plaque.

    Shajil, Chandana / Sathishkumar, Dharshini / Baitule, Amey / George, Anju

    Indian dermatology online journal

    2021  Volume 12, Issue 6, Page(s) 955–956

    Language English
    Publishing date 2021-11-22
    Publishing country India
    Document type Journal Article
    ZDB-ID 2585814-2
    ISSN 2249-5673 ; 2229-5178
    ISSN (online) 2249-5673
    ISSN 2229-5178
    DOI 10.4103/idoj.IDOJ_5_21
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  8. Article ; Online: Spontaneous splenic rupture: A rare complication in eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome).

    Shajil, Chandana / Sathishkumar, Dharshini / George, Krupa / Thomas, Meera

    Indian journal of dermatology, venereology and leprology

    2022  Volume 88, Issue 3, Page(s) 392–395

    MeSH term(s) Churg-Strauss Syndrome/complications ; Churg-Strauss Syndrome/diagnosis ; Granulomatosis with Polyangiitis/complications ; Humans ; Immunosuppressive Agents ; Splenic Rupture/complications
    Chemical Substances Immunosuppressive Agents
    Language English
    Publishing date 2022-04-20
    Publishing country United States
    Document type Letter
    ZDB-ID 416068-x
    ISSN 0973-3922 ; 0019-5162 ; 0378-6323
    ISSN (online) 0973-3922
    ISSN 0019-5162 ; 0378-6323
    DOI 10.25259/IJDVL_584_20
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    Zs.A 85: Show issues Location:
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  9. Article ; Online: Learning to pop blisters in epidermolysis bullosa with a simple model.

    Sathishkumar, Dharshini / Jacob, Anandha Ruby

    Pediatric dermatology

    2020  Volume 37, Issue 6, Page(s) 1215–1217

    Abstract: Epidermolysis bullosa (EB) is a genetic disorder with skin fragility resulting in easy blistering of skin and mucous membranes. A plane of cleavage exists even where there is no visible blister, so new blisters should be drained as soon as possible to ... ...

    Abstract Epidermolysis bullosa (EB) is a genetic disorder with skin fragility resulting in easy blistering of skin and mucous membranes. A plane of cleavage exists even where there is no visible blister, so new blisters should be drained as soon as possible to prevent their expansion. Although, learning how to drain blisters safely and painlessly without introducing infection is essential, it can be a major challenge, especially for new parents and children. To avoid demonstrating the technique directly on patient's skin, we have devised a simple teaching aid simulating a hand and forearm with multiple blisters, created with readily available materials. In our experience, we have found this low-cost model to be extremely useful to teach patients, families, and professional groups, how to drain EB blisters and it provides an effective, low-cost, painless substitute for real-life blisters, empowering parents and engaging children.
    MeSH term(s) Blister/etiology ; Child ; Epidermolysis Bullosa/complications ; Humans ; Mucous Membrane ; Skin
    Language English
    Publishing date 2020-09-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605539-4
    ISSN 1525-1470 ; 0736-8046
    ISSN (online) 1525-1470
    ISSN 0736-8046
    DOI 10.1111/pde.14379
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  10. Article ; Online: Self-healing cutaneous nodules with fever and arthritis: worrisome presentation of a benign disorder.

    Chiramel, Minu J / Sathishkumar, Dharshini / T, Sathish Kumar / Telugu, Ramesh B

    Clinical and experimental dermatology

    2022  Volume 47, Issue 10, Page(s) 1890–1892

    Abstract: A 4-year-old boy with extensive papules and nodules with arthritis was evaluated and followed up. In spite of the initial worrisome presentation, the lesions showed near-complete resolution over a 2-year follow-up period. Click here for the corresponding ...

    Abstract A 4-year-old boy with extensive papules and nodules with arthritis was evaluated and followed up. In spite of the initial worrisome presentation, the lesions showed near-complete resolution over a 2-year follow-up period. Click here for the corresponding questions to this CME article.
    MeSH term(s) Arthritis ; Child, Preschool ; Fever/etiology ; Humans ; Male ; Skin Neoplasms
    Language English
    Publishing date 2022-08-09
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 195504-4
    ISSN 1365-2230 ; 0307-6938
    ISSN (online) 1365-2230
    ISSN 0307-6938
    DOI 10.1111/ced.15272
    Database MEDical Literature Analysis and Retrieval System OnLINE

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