𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Baller-Gerold syndrome associated with congenital hydrocephalus

✍ Scribed by Lewis, M. E. Suzanne ;Rosenbaum, Peter L. ;Paes, Bosco A.

Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
409 KB
Volume
40
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Fanconi anemia in brothers initially dia
Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome
✍ Rossbach, Hans-Christoph; Sutcliffe, Maxine J.; Haag, Mary M.; Grana, Nanette H. πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 12 KB πŸ‘ 2 views

T w o brothers with presumed Baller-Gerold syndrome, one of whom was previously diagnosed with the association of vertebral, cardiac, renal, limb anomalies, anal atresia, tracheo-esophageal fistula (VACTERL) association with hydrocephalus, were evaluated for chromosome breakage because of severe thr

Long first metacarpal in monozygotic twi
Long first metacarpal in monozygotic twins with probable Baller-Gerold syndrome
✍ Franceschini, Piergiorgio; Licata, Domenico; Guala, Andrea; Di Cara, Giuseppe; S πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 41 KB πŸ‘ 2 views

We report on a pair of monozygotic twins with probable Baller-Gerold syndrome (BGS). Twin A had severe coronal craniosynostosis. Twin B had right radioulnar and ipsilateral first metacarpal hypoplasia. Both had bilateral fifth finger clinodactyly. Assuming that the twins were truly monozygotic, a si

Congenital heart disease associated with
Congenital heart disease associated with sporadic Kallmann syndrome
✍ Cortez, Alan B. ;Galindo, Alvaro ;Arensman, Frederick W. ;van Dop, Cornelis πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 409 KB πŸ‘ 2 views

A 17-year-old boy with Kallmann syndrome had complex congenital heart disease that included double-outlet right ventricle, d-malposition of the great arteries, right aortic arch, and hypoplastic main pulmonary artery. He had neurosensory hearing loss and mental retardation. The 7 previously reported