𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Multiple skeletal anomalies in the “13q-” syndrome

✍ Scribed by J. Chemke; E. Fishel; M. Zalish; M. Sagiv


Publisher
Springer
Year
1978
Tongue
English
Weight
1012 KB
Volume
128
Category
Article
ISSN
0340-6997

No coin nor oath required. For personal study only.

✦ Synopsis


A patient with the "13q-" syndrome is reported. The typical association of congenital malformations was found. Multiple and unusual skeletal anomalies included absent thumbs, club-feet, coxa vara, diastasis of the pubic symphisis and extensive spina bifida occulta. These appear to be part of the multiple system involvement due to the chromosomal deletion. Chromosome analysis is indicated in patients with multiple skeletal anomalies, especially if the thumbs and radial axis are involved.


📜 SIMILAR VOLUMES


Syndrome of total alopecia, multiple ske
✍ van Gelderen, H. H. ;Opitz, John M. 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 298 KB 👁 2 views

## Abstract This is a report of a 16‐year‐old boy with mental deficiency, shortness of stature, peculiar face and skull, multiple skeletal anomalies, limb contractures, total alopecia, and probable hypothalamic hypogonadism. A striking resemblance exists between this case and a female adolescent de

New multiple congenital anomalies: Menta
✍ Borochowitz, Zvi ;Pavone, Lorenzo ;Mazor, Galia ;Rizzo, Renata ;Dar, Hanna 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 933 KB

Five unrelated patients (a male and 4 females) were affected with a previously undefined multiple congenital anomalies/mental retardation syndrome which has been designated the facio-cutaneous-skeletal (FCS) syndrome and which includes mental retardation with specific sociable, humorous behavior, ch

Multiple congenital anomalies/mental ret
✍ Steinbach, P. ;Wolf, M. ;Schmidt, H. 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 353 KB 👁 2 views

## Abstract A severely retarded male infant was found to have a previously undescribed multiple congenital anomalies/mental retardation (MCA/MR) syndrome including microdolichocephaly, prominence of metopic suture, coarse scalp hair, epicanthus, anteverted nostrils, micrognathia, posteriorly angula