Expanding the phenotypic spectrum of PORCN variants in two males with syndromic microphthalmia

Paul D Brady, Hilde Van Esch, Nathalie Fieremans, Guy Froyen, Anne Slavotinek, Jan Deprest, Koenraad Devriendt, Joris R Vermeesch

Onderzoeksoutput: Articlepeer review

24 Citaten (Scopus)

Samenvatting

Variants in PORCN are a cause of Goltz-Gorlin syndrome or Focal Dermal Hypoplasia, an X-linked dominant disorder affecting heterozygous females and until now considered to be embryonic lethal in males. Exome sequencing was performed in a family in which two male siblings were characterized by microphthalmia and additional congenital anomalies including diaphragmatic hernia, spina bifida and cardiac defects. Surprisingly, we identified a maternally inherited variant in PORCN present in both males as well as in two female siblings. This represents the first finding of a PORCN variant in non-mosaic males affected with Goltz-Gorlin syndrome. The apparently asymptomatic mother showed extreme skewing of X-inactivation (90%), an asymptomatic female sibling showed skewing of 88%, and the second female sibling affected with cutis aplasia of the scalp showed X-inactivation considered within the normal range.

Originele taal-2English
Pagina's (van-tot)551-4
Aantal pagina's4
TijdschriftEuropean Journal of Human Genetics
Volume23
Nummer van het tijdschrift4
DOI's
StatusPublished - apr 2015

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