We describe an infant with congenital vocal cord paralysis born to consanguineous parents. While autosomal dominant and X-linked inheritance have been previously reported in this condition, we conclude that the degree of parental consanguinity in this case strongly suggests autosomal recessive inher
Severe brain and limb defects with possible autosomal recessive inheritance: A series of six cases and review of the literature
✍ Scribed by Labrune, Philippe; Trioche, Pascale; Fallet-Bianco, Catherine; Roume, Joëlle; Narcy, Françoise; Le Merrer, Martine
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 22 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0148-7299
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✦ Synopsis
Six fetuses with normal chromosomes were found to have severe craniofacial, limb, and visceral malformations during the second trimester of pregnancy. Two of these fetuses were monozygotic twins while a third one had a healthy dizygotic twin brother. A case with familial recurrence was also observed. Autopsy and skeletal radiographs suggested several diagnoses such as neural tube defect with limb defects or XK aprosencephaly.The development of these severe conditions in monozygotic twins and familial recurrence emphasize the difficulties of genetic counseling in such situations. These cases may suggest autosomal recessive inheritance.
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