𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Trisomy 9 syndrome: Report of a case with Crohn disease and review of the literature

✍ Scribed by Wooldridge, Jamie ;Zunich, Janice


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
613 KB
Volume
56
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Sebastian syndrome: Case report and revi
✍ Young, Guy; Luban, Naomi L.C.; White, James G. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 195 KB πŸ‘ 1 views

Macrothrombocytopenias (MTCP) are a heterogeneous group of disorders associated with thrombocytopenia and giant platelets, and may include other clinical or laboratory findings such as hereditary nephritis, sensorineural deafness, leukocyte inclusions, and cataracts. Patients with MTCP may have mild

Fryns syndrome: Case report and review o
✍ Gulseren Yucesoy; Yigit Cakiroglu; Eray Caliskan πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 155 KB πŸ‘ 1 views

## Abstract Fryns syndrome (FS) is a rare malformation. We report a case of FS referred to our clinic at 27 weeks' gestation with a diagnosis of congenital diaphragmatic hernia. Sonographic examination of the fetus revealed a left‐sided diaphragmatic hernia, pulmonary hypoplasia, and a median orofa

A girl with metopic synostosis and triso
✍ Ebru Aypar; M. Selman Yildirim; Ahmet Sert; Ilhan Ciftci; Dursun Odabas πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 175 KB πŸ‘ 1 views

## Abstract Trisomy 13, or Patau syndrome is a rare chromosomal disorder characterized by a triad of cleft lip and palate, postaxial polydactyly and microcephaly. Complete, partial, or mosaic forms of the disorder can occur. Mosaic trisomy 13 is very rare, it occurs in only 5% of all patients with