An infantile case of Zellweger syndrome presented with Kabuki-like phenotype.

TitleAn infantile case of Zellweger syndrome presented with Kabuki-like phenotype.
Publication TypeJournal Article
Year of Publication2011
AuthorsEzgu E, Eminoglu T, Okur I, Gunduz M, Tumer L, Hasanoglu A, Dalgic B
JournalGenetic counseling (Geneva, Switzerland)
Volume22
Issue2
Pagination217-20
Date Published2011
ISSN1015-8146
KeywordsAbnormalities, Multiple, Child, Preschool, Diagnosis, Differential, Face, Hematologic Diseases, Humans, Liver, Liver Function Tests, Male, Phenotype, Vestibular Diseases, Zellweger Syndrome
Abstract

Zellweger syndrome is a peroxisomal disorder resulting from the mutations in PEX genesi generally presenting in the neonatal period with profound hypotonia seizures, inability to feed, liver cysts with hepatic dysfunction, chondrodysplasia punctata. Kabuki make-up syndrome is a multiple congenitali anomalies and mental retardation syndrome with characteristic facial appearance, skeletal abnormalities, dermatoglyphic abnormalities, mental retardation and short stature. Abnormal liver functions and some atypicali findings were also reported in some patients with Kabuki syndrome. In this report a case with late onset Zellweger syndrome who had some phenotypical findings which are also seen in Kabuki Syndrome will be presented. The inclusion of Zellweger syndrome into the differential diagnosis of the patients with Kabuki-like phenotypei in addition to abnormal liver functions is emphasized.

Alternate JournalGenet. Couns.
Citation Key940
PubMed ID21848015