Literature DB >> 24066991

Biotinidase deficiency: an atypical presentation.

Sujatha Jagadeesh1, Beena Suresh, Suresh Seshadri, Yoichi Suzuki.   

Abstract

Biotinidase deficiency is a rare metabolic disorder which can cause dermatological manifestations and lead to severe neurological sequelae if untreated. Holocarboxylase synthetase deficiency also has similar manifestations and needs to be differentiated. We present a neonate who had atypical early onset symptoms and was diagnosed to have biotinidase deficiency. Copyright 2012, NMJI.

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Year:  2013        PMID: 24066991

Source DB:  PubMed          Journal:  Natl Med J India        ISSN: 0970-258X            Impact factor:   0.537


  2 in total

1.  Status of Newborn Screening and Inborn Errors of Metabolism in India.

Authors:  Seema Kapoor; B K Thelma
Journal:  Indian J Pediatr       Date:  2018-05-07       Impact factor: 1.967

2.  Molecular Background and Disease Prevalence of Biotinidase Deficiency in a Polish Population-Data Based on the National Newborn Screening Programme.

Authors:  Aleksandra Jezela-Stanek; Lidia Suchoń; Agnieszka Sobczyńska-Tomaszewska; Kamila Czerska; Katarzyna Kuśmierska; Joanna Taybert; Mariusz Ołtarzewski; Jolanta Sykut-Cegielska
Journal:  Genes (Basel)       Date:  2022-04-29       Impact factor: 4.141

  2 in total

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