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Premium Chediak–Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1
Author(s)
Manoli Irini,
Golas Gretchen,
Westbroek Wendy,
Vilboux Thierry,
Markello Thomas C.,
Introne Wendy,
Maynard Dawn,
Pederson Ben,
Tsilou Ekaterini,
Jordan Michael B.,
Hart P. Suzanne,
White James G.,
Gahl William A.,
Huizing Marjan
Publication year2010
Publication title
american journal of medical genetics part a
Resource typeJournals
PublisherWiley Subscription Services
Abstract Chediak–Higashi syndrome (CHS) is a rare autosomal recessive disease characterized by variable oculocutaneous albinism, immunodeficiency, mild bleeding diathesis, and an accelerated lymphoproliferative state. Abnormal lysosome‐related organelle membrane function leads to the accumulation of large intracellular vesicles in several cell types, including granulocytes, melanocytes, and platelets. This report describes a severe case of CHS resulting from paternal heterodisomy of chromosome 1, causing homozygosity for the most distal nonsense mutation (p.E3668X, exon 50) reported to date in the LYST/CHS1 gene. The mutation is located in the WD40 region of the CHS1 protein. The patient's fibroblasts expressed no detectable CHS1. Besides manifesting the classical CHS findings, the patient exhibited hypotonia and global developmental delays, raising concerns about other effects of heterodisomy. An interstitial 747 kb duplication on 6q14.2–6q14.3 was identified in the propositus and paternal samples by comparative genomic hybridization. SNP genotyping revealed no additional whole chromosome or segmental isodisomic regions or other dosage variations near the crossover breakpoints on chromosome 1. Unmasking of a separate autosomal recessive cause of developmental delay, or an additive effect of the paternal heterodisomy, could underlie the severity of the phenotype in this patient. Published 2010 Wiley‐Liss, Inc.
Subject(s)albinism , biology , chédiak–higashi syndrome , gene , genetics , hypotonia , missense mutation , mutation , nonsense mutation , oculocutaneous albinism
Language(s)English
SCImago Journal Rank1.064
H-Index112
eISSN1552-4833
pISSN1552-4825
DOI10.1002/ajmg.a.33389

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