𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Autosomal recessive hydrocephalus with third ventricle obstruction

✍ Scribed by Chow, C. W. ;McKelvie, P. A. ;Anderson, R. McD. ;Phelan, E. M. D. ;Klug, G. L. ;Rogers, J. G.


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
453 KB
Volume
35
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Sibs with Axenfeld-Rieger anomaly, hydro
✍ Moog, U.; Bleeker-Wagemakers, E.M.; Crobach, P.; Vles, J.S.H.; Schrander-Stumpel πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 22 KB πŸ‘ 2 views

The Axenfeld-Rieger anomaly is a defect of the anterior chamber of the eye affecting the angle structures. If accompanied by hypodontia, midface hypoplasia, and umbilical anomalies, the designation ''Rieger syndrome'' is appropriate. Both conditions are autosomal dominant traits. The Axenfeld-Rieger

Bilateral sensorineural deafness and hyd
✍ Chudley, Albert E.; McCullough, Carol; McCullough, David W. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 442 KB πŸ‘ 1 views

We identified a Canadian-Mennonite family in which a brother and sister have hydrocephalus due to obstruction at the foramen of Monro and profound bilateral sensorineural deafness. This appears to be a unique combination of anomalies and, to our knowledge, has not been reported previously. Both pare

Autosomal recessive acro-fronto-facio-na
✍ Myriam Chaabouni; Faouzi Maazoul; Amira Ben Hamida; Moncef Berhouma; Zahra Marra πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 87 KB πŸ‘ 1 views

## Abstract We report on a 22‐day‐old Tunisian boy born to consanguineous (first‐cousin) parents (F = 1/16). The patient presents wide forehead with frontal encephalocele, wide anterior fontanel, marked hypertelorism, coloboma of the upper lids, proptosis, congenital glaucoma, broad nose, syndactyl