TY - JOUR
T1 - Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita
AU - Frints, Suzanna G. M.
AU - Hennig, Friederike
AU - Colombo, Roberto
AU - Jacquemont, Sebastien
AU - Terhal, Paulien
AU - Zimmerman, Holly H.
AU - Hunt, David
AU - Mendelsohn, Bryce A.
AU - Kordaß, Ulrike
AU - Webster, Richard
AU - Sinnema, Margje
AU - Abdul-Rahman, Omar
AU - Suckow, Vanessa
AU - Fernández-Jaén, Alberto
AU - van Roozendaal, Kees
AU - Stevens, Servi J. C.
AU - Macville, Merryn V. E.
AU - Al-Nasiry, Salwan
AU - van Gassen, Koen
AU - Utzig, Norbert
AU - Koudijs, Suzanne M.
AU - McGregor, Lesley
AU - Maas, Saskia M.
AU - Baralle, Diana
AU - Dixit, Abhijit
AU - Wieacker, Peter
AU - Lee, Marcus
AU - Lee, Arthur S.
AU - Engle, Elizabeth C.
AU - Houge, Gunnar
AU - Gradek, Gyri A.
AU - Douglas, Andrew G. L.
AU - Longman, Cheryl
AU - Joss, Shelagh
AU - Velasco, Danita
AU - Hennekam, Raoul C.
AU - Hirata, Hiromi
AU - Kalscheuer, Vera M.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Pathogenic variants in the X-linked gene ZC4H2, which encodes a zinc-finger protein, cause an infrequently described syndromic form of arthrogryposis multiplex congenita (AMC) with central and peripheral nervous system involvement. We present genetic and detailed phenotypic information on 23 newly identified families and simplex cases that include 19 affected females from 18 families and 14 affected males from nine families. Of note, the 15 females with deleterious de novo ZC4H2 variants presented with phenotypes ranging from mild to severe, and their clinical features overlapped with those seen in affected males. By contrast, of the nine carrier females with inherited ZC4H2 missense variants that were deleterious in affected male relatives, four were symptomatic. We also compared clinical phenotypes with previously published cases of both sexes and provide an overview on 48 males and 57 females from 42 families. The spectrum of ZC4H2 defects comprises novel and recurrent mostly inherited missense variants in affected males, and de novo splicing, frameshift, nonsense, and partial ZC4H2 deletions in affected females. Pathogenicity of two newly identified missense variants was further supported by studies in zebrafish. We propose ZC4H2 as a good candidate for early genetic testing of males and females with a clinical suspicion of fetal hypo-/akinesia and/or (neurogenic) AMC.
AB - Pathogenic variants in the X-linked gene ZC4H2, which encodes a zinc-finger protein, cause an infrequently described syndromic form of arthrogryposis multiplex congenita (AMC) with central and peripheral nervous system involvement. We present genetic and detailed phenotypic information on 23 newly identified families and simplex cases that include 19 affected females from 18 families and 14 affected males from nine families. Of note, the 15 females with deleterious de novo ZC4H2 variants presented with phenotypes ranging from mild to severe, and their clinical features overlapped with those seen in affected males. By contrast, of the nine carrier females with inherited ZC4H2 missense variants that were deleterious in affected male relatives, four were symptomatic. We also compared clinical phenotypes with previously published cases of both sexes and provide an overview on 48 males and 57 females from 42 families. The spectrum of ZC4H2 defects comprises novel and recurrent mostly inherited missense variants in affected males, and de novo splicing, frameshift, nonsense, and partial ZC4H2 deletions in affected females. Pathogenicity of two newly identified missense variants was further supported by studies in zebrafish. We propose ZC4H2 as a good candidate for early genetic testing of males and females with a clinical suspicion of fetal hypo-/akinesia and/or (neurogenic) AMC.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85070930315&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/31206972
U2 - https://doi.org/10.1002/humu.23841
DO - https://doi.org/10.1002/humu.23841
M3 - Article
C2 - 31206972
SN - 1059-7794
VL - 40
SP - 2270
EP - 2285
JO - Human Mutation
JF - Human Mutation
IS - 12
ER -