𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Recessive polycystic kidney disease and congenital hypertrophic pyloric stenosis

✍ Scribed by A. K. Gupta

Publisher
Springer-Verlag
Year
1991
Tongue
English
Weight
63 KB
Volume
21
Category
Article
ISSN
0301-0449

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Congenital mesoblastic nephroma, nephroc
Congenital mesoblastic nephroma, nephrocalcinosis, and hypertrophic pyloric stenosis
✍ Javier C. Angulo; Jose I. Lopez; Cosme EreΓ±ao; Nicolas Flores πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 373 KB

## Abstract A cellular variant of congenital mesoblastic nephroma (CMN) occurring in a newborn is presented. Coincidental findings were congenital hypertrophic pyloric stenosis (CHPS) and nephrocalcinotic hypercalcemia that reverted after nephrectomy. As of the day of writing, this multiple associa

PKHD1 mutations in autosomal recessive p
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
✍ Carsten Bergmann; Jan Senderek; Fabian KΓΌpper; Frank Schneider; Christian Dornia πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 277 KB

## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal-and liverrelated morbidity and mortality. The clinical spectrum is widely variable. About 30 to 50% of affected individuals die in the neonatal period, while others survive

Autosomal recessive and dominant forms o
Autosomal recessive and dominant forms of polycystic kidney disease are not allelic
✍ Brunhilde Wirth; K. Zerres; M. Fischbach; Dorothea Claus; H. P. H. Neumann; T. L πŸ“‚ Article πŸ“… 1987 πŸ› Springer 🌐 English βš– 169 KB

Linkage analysis has been carried out in 11 kindreds with autosomal recessive polycystic kidney disease (ARPKD) using the genetic marker 3'HVR, closely linked (theta = 0.05) to the gene of the autosomal dominant type. Close linkage (theta less than or equal to 0.20) between the locus of the marker a