Aprosencephaly is a rare, lethal malformation sequence of the central nervous system that has been attributed to a postneuralation encephaloclastic process. We describe autopsy findings consistent with aprosencephaly in 2 fetuses conceived from a consanguineous mating (first cousins). Both showed an
Holoprosencephaly and endocrine dysgenesis in brothers
โ Scribed by Begleiter, Michael L. ;Harris, David J. ;Optiz, John M.
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 244 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
We report on three brothers with renal tubular dysgenesis and absent nipples, each also had other malformations including preauricular pits and a preauricular tag, branchial clefts, choanal atresia, pulmonary lobation anomaly, ventricular septal defect, type IIB interrupted aortic arch, absent gallb
## Abstract **BACKGROUND:** Exposure of pregnant outbred CDโ1 mice to methanol during the period of gastrulation results in exencephaly, cleft palate, and cervical vertebra malformations [Rogers and Mole, Teratology 55: 364, 1997], while inbred C57BL/6J mice are sensitive to the teratogenicity of e