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  1. Article: Clinical and Genetic Profile of Indian Children with Primary Hyperoxaluria.

    Pinapala, A / Garg, M / Kamath, N / Iyengar, A

    Indian journal of nephrology

    2017  Volume 27, Issue 3, Page(s) 222–224

    Abstract: Primary hyperoxaluria (PH) has heterogeneous renal manifestations in infants and children. This often leads to delay in diagnosis. In the past 3 years, genetic samples were sent for seven children with a clinical diagnosis of PH. Their medical records ... ...

    Abstract Primary hyperoxaluria (PH) has heterogeneous renal manifestations in infants and children. This often leads to delay in diagnosis. In the past 3 years, genetic samples were sent for seven children with a clinical diagnosis of PH. Their medical records were reviewed for clinical presentation and outcomes. Of the seven children, three were males. The median age of presentation was 4.9 years with the youngest presenting at 3 months of age. Nephrolithiasis, the most common presentation was associated with renal dysfunction in two children. Two children with no significant history presented in end-stage renal disease (ESRD). The sibling of one of the children in ESRD, with a history of consanguinity in parents, was screened for asymptomatic nephrolithiasis. Bilateral multiple renal calculi were found in majority of children followed by echogenic kidneys on ultrasound examination. Genetic analysis suggested PH Type 1 in five children and type 2 in two children. The mutations detected in our cohort were different from the previously reported common mutations. There was no obvious genotype-phenotype correlation noticed. Three children in ESRD are on maintenance dialysis. Nephrolithiasis being a common presentation of PH needs prompt evaluation. Mutations are generally population specific, and whole gene sequence analysis is critical in diagnosis.
    Language English
    Publishing date 2017-05-09
    Publishing country India
    Document type Case Reports
    ZDB-ID 2134388-3
    ISSN 1998-3662 ; 0971-4065
    ISSN (online) 1998-3662
    ISSN 0971-4065
    DOI 10.4103/0971-4065.202831
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Clofazimine in

    Pinapala, Archana / Koh, Lee Jin / Ng, Kar-Hui / Tambyah, Paul A / Yap, Hui-Kim

    Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis

    2020  Volume 41, Issue 1, Page(s) 104–109

    Abstract: Peritonitis- and catheter-related infections due to nontuberculous mycobacteria (NTM) ... ...

    Abstract Peritonitis- and catheter-related infections due to nontuberculous mycobacteria (NTM) including
    MeSH term(s) Adult ; Child ; Clofazimine/therapeutic use ; Drug Therapy, Combination ; Female ; Humans ; Leprostatic Agents/therapeutic use ; Mycobacterium Infections, Nontuberculous/diagnosis ; Mycobacterium Infections, Nontuberculous/drug therapy ; Mycobacterium abscessus ; Peritoneal Dialysis/adverse effects ; Peritonitis/diagnosis ; Peritonitis/drug therapy ; Peritonitis/etiology
    Chemical Substances Leprostatic Agents ; Clofazimine (D959AE5USF)
    Language English
    Publishing date 2020-03-09
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 645010-6
    ISSN 1718-4304 ; 0896-8608
    ISSN (online) 1718-4304
    ISSN 0896-8608
    DOI 10.1177/0896860820909702
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Clinical and genetic profile of Indian children with primary hyperoxaluria

    A Pinapala / M Garg / N Kamath / A Iyengar

    Indian Journal of Nephrology, Vol 27, Iss 3, Pp 222-

    2017  Volume 224

    Abstract: Primary hyperoxaluria (PH) has heterogeneous renal manifestations in infants and children. This often leads to delay in diagnosis. In the past 3 years, genetic samples were sent for seven children with a clinical diagnosis of PH. Their medical records ... ...

    Abstract Primary hyperoxaluria (PH) has heterogeneous renal manifestations in infants and children. This often leads to delay in diagnosis. In the past 3 years, genetic samples were sent for seven children with a clinical diagnosis of PH. Their medical records were reviewed for clinical presentation and outcomes. Of the seven children, three were males. The median age of presentation was 4.9 years with the youngest presenting at 3 months of age. Nephrolithiasis, the most common presentation was associated with renal dysfunction in two children. Two children with no significant history presented in end-stage renal disease (ESRD). The sibling of one of the children in ESRD, with a history of consanguinity in parents, was screened for asymptomatic nephrolithiasis. Bilateral multiple renal calculi were found in majority of children followed by echogenic kidneys on ultrasound examination. Genetic analysis suggested PH Type 1 in five children and type 2 in two children. The mutations detected in our cohort were different from the previously reported common mutations. There was no obvious genotype-phenotype correlation noticed. Three children in ESRD are on maintenance dialysis. Nephrolithiasis being a common presentation of PH needs prompt evaluation. Mutations are generally population specific, and whole gene sequence analysis is critical in diagnosis.
    Keywords Nephrocalcinosis ; nephrolithiasis ; primary hyperoxaluria ; Diseases of the genitourinary system. Urology ; RC870-923 ; Specialties of internal medicine ; RC581-951 ; Internal medicine ; RC31-1245 ; Medicine ; R
    Subject code 610
    Language English
    Publishing date 2017-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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