𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A family with nephronophthisis – medullary cystic disease complex

✍ Scribed by M. Arakawa; Jun Chiba; Yasuhiko Sasaki; Mituyoshi Narita; Hiroshi Satou; Takao Saitou

Book ID
106288711
Publisher
Springer
Year
1999
Tongue
English
Weight
323 KB
Volume
3
Category
Article
ISSN
1342-1751

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Sonographic findings in familial juvenil
Sonographic findings in familial juvenile nephronophthisis–medullary cystic disease complex
✍ Chuang, Yung-Fang; Tsai, Tsuen-Chiuan 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 169 KB 👁 1 views

## Purpose: Familial juvenile nephronophthisis-medullary cystic disease complex (jn-mcd) is an autosomal inherited renal disease with insidious symptoms that ultimately progresses to renal failure. we describe the abnormal sonographic findings in jn-mcd at various stages of the disease in a taiwane

Medullary cystic kidney disease with hyp
Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: No allelism with nephronophthisis type 1
✍ Stavrou, Christoforos; Pierides, Alkis; Zouvani, Ioanna; Kyriacou, Kyriacos; Ant 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 46 KB 👁 2 views

We describe a large Cypriot family with an interstitial type of nephropathy, inherited as an autosomal dominant trait that led to end stage renal failure between 51 to 78 years of age (mean 62.2 years). Twenty-three people are known to be affected, but several younger relatives with normal renal fun