Meckel-Gruber syndrome, also known as dysencephalia splachnocystica, was originally described by Meckel in 1822, later by Gruber, and more recently by Opitz and Howe. More than 50 cases of this severe disorder have been reported.' This syndrome is characterized by microcephaly secondary to cerebral
✦ LIBER ✦
Atypical Rokitansky-Kauster-Hauser syndrom
✍ Scribed by H. Chelli; D. Chelli; M.B. Chennouffi; A. Souki; E. Sfar
- Book ID
- 117125457
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 153 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0020-7292
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