Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome?
โ Scribed by Mary C. O'Driscoll; Kim Jenny; Sulagna Saitta; William B. Dobyns; Karen W. Gripp
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 189 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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๐ SIMILAR VOLUMES
Most reported familial cases of agenesis of the corpus callosum have followed either an autosomal recessive or an X-linked recessive pattern of inheritance. To the best of our knowledge, there is only one previous report of a family showing clear-cut autosomal dominant inheritance. We present the se
## Abstract ## BACKGROUND: Pai syndrome (PS) is a rare regional developmental defect of the face, mainly characterized by the variable association of midline cleft of the upper lip (MCL), duplicated maxillary median frenulum, and midline facial cutaneous and midanterior alveolar process polyps. It