A new autosomal recessive congenital contractural syndrome in an Israeli Bedouin kindred

D Landau, A Mishori‐Dery… - American Journal of …, 2003 - Wiley Online Library
D Landau, A Mishori‐Dery, R Hershkovitz, G Narkis, K Elbedour, R Carmi
American Journal of Medical Genetics Part A, 2003Wiley Online Library
We describe 23 cases with a syndrome of congenital contractures belonging to a large,
inbred Israeli‐Bedouin kindred. The phenotype described is similar to the Finnish type lethal
congenital contracture syndrome yet differs in the following ways: by some additional
craniofacial/ocular findings, by the lack of hydrops, multiple pterygia, and fractures, and by
the normal duration of pregnancy. The major unique and previously undescribed clinical
feature in our patients is a markedly distended urinary bladder as well as other urinary …
Abstract
We describe 23 cases with a syndrome of congenital contractures belonging to a large, inbred Israeli‐Bedouin kindred. The phenotype described is similar to the Finnish type lethal congenital contracture syndrome yet differs in the following ways: by some additional craniofacial/ocular findings, by the lack of hydrops, multiple pterygia, and fractures, and by the normal duration of pregnancy. The major unique and previously undescribed clinical feature in our patients is a markedly distended urinary bladder as well as other urinary abnormalities. The vast majority of the cases died shortly after birth. Sonographic prenatal diagnosis was possible as early as 15 weeks gestation by demonstrating fetal akinesia, limb contractures, hydramnios, and distended urinary bladder. Linkage to 5q and 9q34 loci has been excluded. © 2002 Wiley‐Liss, Inc.
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