| Literature DB >> 30561130 |
Svenja Alter1, Alrun Hotz1, Arne Jahn2, Nataliya Di Donato2, Evelin Schröck2, Martin Smitka3, Maja von der Hagen3, Jens Schallner3, Mario Menschikowski4, Claus Gillitzer3, Martin W Laass3, Judith Fischer1, Andreas Tzschach2.
Abstract
Autosomal recessive keratoderma-ichthyosis-deafness (ARKID) syndrome is a rare multisystem disorder caused by biallelic mutations in VPS33B; only three patients have been reported to date. ARKID syndrome is allelic to arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome (MIM #208085), a severe disorder with early lethality whose phenotypic characteristics also include ichthyosis, hearing loss, severe failure to thrive, platelet dysfunction and osteopenia. We report on an 11-year-old male patient with ARKID syndrome and compound heterozygous VPS33B mutations, one of which [c.1440delG; p.(Arg481Glyfs*11)] was novel. Clinical features of this patient included ichthyosis, palmoplantar keratosis, hearing loss, intellectual disability, unilateral hip dislocation, microcephaly and short stature. He also had copper hepatopathy and exocrine pancreatic insufficiency, features that have so far been associated with neither ARKID nor ARC syndrome. The patient broadens the clinical and molecular spectrum of ARKID syndrome and contributes to genotype-phenotype associations of this rare disorder.Entities:
Keywords: zzm321990VPS33B; arthrogryposis-renal dysfunction-cholestasis syndrome; autosomal recessive keratoderma-ichthyosis-deafness syndrome; copper hepatopathy
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Year: 2018 PMID: 30561130 DOI: 10.1002/ajmg.a.40634
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802