Familial macrocephaly with mesodermal hamartomas is described as a distinct syndrome in nine individuals from four families. Constant manifestations include symmetrical macrocephaly without ventricular enlargement, mild neurological dysfunction. and postnatal growth deceleration. Speech and motor de
✦ LIBER ✦
Syndrome de Bannayan-Zonana d’évolution fatale
✍ Scribed by K. Khadir; A. Eddaoui; S. Chiheb; D. Bourhnane; N. Chaffik; S. Azzouzi; H. Benchikhi
- Book ID
- 116254196
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 552 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0929-693X
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