Literature DB >> 21615476

What syndrome is this? Infantile periorificial and intertriginous dermatitis preceding sepsis-like respiratory failure.

Edward M Esparza1, Alana S Golden, Si H Hahn, Kathleen Patterson, Heather A Brandling-Bennett.   

Abstract

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Year:  2011        PMID： 21615476     DOI： 10.1111/j.1525-1470.2011.01439.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN： 0736-8046            Impact factor:   1.588


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  3 in total

Review 1.  Antenatal and postnatal radiologic diagnosis of holocarboxylase synthetase deficiency: a systematic review.

Authors:  Sahan P Semasinghe Bandaralage; Soheil Farnaghi; Joel M Dulhunty; Alka Kothari
Journal:  Pediatr Radiol       Date:  2016-01-11

2.  Clinical Presentation and Positive Outcome of Two Siblings with Holocarboxylase Synthetase Deficiency Caused by a Homozygous L216R Mutation.

Authors:  T P Slavin; S J Zaidi; C Neal; B Nishikawa; L H Seaver
Journal:  JIMD Rep       Date:  2013-09-13

3.  Paracentric Inversion of Chromosome 21 Leading to Disruption of the HLCS Gene in a Family with Holocarboxylase Synthetase Deficiency.

Authors:  Shane C Quinonez; Andrea H Seeley; Cindy Lam; Thomas W Glover; Bruce A Barshop; Catherine E Keegan
Journal:  JIMD Rep       Date:  2016-08-13
  3 in total

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