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 ✦
Arteriovenous malformation in a patient with Bannayan–Zonana syndrome
✍ Scribed by Jason J Naidich; Neil M Rofsky; Robert Rosen; Nolan Karp
- Book ID
- 114284578
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 161 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0899-7071
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