✦ LIBER ✦

A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother

✍ Scribed by C. Stoll; P. Talon; L. Mengus; M. P. Roth; B. Dott

Book ID: 115089235
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 349 KB
Volume: 28
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.1985.tb00396.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Weaver-like syndrome in a Japanese boy

✍ Masato Tsukahara; Suguru Tanaka; Tadashi Kajii 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 465 KB

Poland-Moebius syndrome in a boy and Pol

Poland-Moebius syndrome in a boy and Poland syndrome in his mother

✍ A. Rojas-Martínez; D. García-Cruz; A. Rodríguez García; J. Sánchez-Corona; F. Ri 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB

Novel findings in a patient with Weaver

Novel findings in a patient with Weaver or a Weaver-like syndrome

✍ Scarano, Gioacchino; Monica, Matteo Della; Lonardo, Fortunato; Neri, Giovanni 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 38 KB 👁 2 views

W e report on a young male patient with an overgrowth syndrome, who had normal birth weight. He had a number of manifestations typical of the Weaver syndrome (WS), such as advanced bone age, peculiar craniofacial appearance, and camptodactyly. He also showed severe mental and speech retardation and

Bazex–Dupré–Christol Syndrome in a 1-Yea

Bazex–Dupré–Christol Syndrome in a 1-Year-Old Boy and His Mother

✍ ANDREZZA CAMARINHA NAPOLITANO BARCELOS; MARCELLO MENTA SIMONSEN NICO 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 193 KB

Severe craniofacial sclerosis with multi

Severe craniofacial sclerosis with multiple anomalies in a boy and his mother

✍ G. Currarino; J. M. Friedman 📂 Article 📅 1986 🏛 Springer-Verlag 🌐 English ⚖ 842 KB

Non-syndromic hemihyperplasia in a male

Non-syndromic hemihyperplasia in a male and his mother

✍ Slavotinek, Anne M. ;Collins, Michael T. ;Muenke, Maximilian 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 1 views

## Abstract We present two family members with non‐syndromic hemihyperplasia (HHP), which developed in adolescence. We have reviewed reported familial cases of HHP and conclude that presentation is similar to sporadi cases and that all affected family members have been related through a maternal re