𝔖 Bobbio Scriptorium
✦   LIBER   ✦

PP-81. Bartter syndrome a neonatal presentation: A report of three cases

✍ Scribed by Hese Cosar; Ali Kanık; Aydın Erdemir; Ebru Turkoglu; Zelal Kahramaner; Sumer Sutcuoglu; Onder Yavascan; Esra Arun Ozer

Book ID
113572707
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
57 KB
Volume
86
Category
Article
ISSN
0378-3782

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Anophthalmia-Waardenburg syndrome: A rep
Anophthalmia-Waardenburg syndrome: A report of three cases
✍ Suyugül, Zuhal; Seven, Mehmet; Hacihanefioğlu, Seniha; Kartal, Aysin; Suyugül, N 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 55 KB 👁 3 views

W e report on 2 Turkish families with children who had bilateral anophthalmia, upper and lower limb abnormalities, mental retardation and consanguineous parents. We have evaluated the 2 cases in the first family and the only case in the second as anophthalmia-Waardenburg syndrome. This is an extreme

Filippi syndrome: Report of three additi
Filippi syndrome: Report of three additional cases
✍ Williams, Marc S.; Williams, Janet L.; Wargowski, David S.; Pauli, Richard M.; P 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 48 KB 👁 3 views

Filippi syndrome is an autosomal recessive condition characterized by variable soft tissue syndactyly of the fingers and toes, microcephaly, pre-and postnatal growth retardation, mildly abnormal craniofacial appearance, and mental retardation. We report on three unrelated individuals with Filippi sy