𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Acro-renal polytopic defect

✍ Scribed by Hegde, Hardally R. ;Leung, Alexander K. C. ;Robson, Wm. Lane M.


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
86 KB
Volume
39
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


New variant of acro-renal field defect
✍ Scheuerman, Oded ;Horev, Gadi ;Merlob, Paul 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 94 KB

## Abstract We describe two patients with a new variant of acro‐renal field defect. The first was a full‐term, small‐for‐gestational‐age female infant who showed preaxial polydactyly of the right hand and horseshoe kidney on abdominal ultrasonographic examination. In addition, there was a single um

Acro-renal-mandibular syndrome
✍ Halal, Fahed ;Desgranges, Marie-Françoise ;Leduc, Bernard ;Thêorét, Gilles ;Bett 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 477 KB
Severe acro-renal-uterine-mandibular syn
✍ Evans, Jane A. ;Phillips, Susan ;Reed, Martin ;Chodirker, Bernard N. 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 459 KB

Although limb and renal defects occur together in a variety of patterns of multiple malformations, familial cases of acro-renal disorders are rare. In 1980, Halal et al. [Am J Med Genet 5:277-284] described two sisters with unusual limb deficiencies, renal anomalies, and mandibular hypoplasia and te

Further delineation of the acro-renal-oc
✍ Aalfs, Cora M.; van Schooneveld, Mary J.; van Keulen, Estéban M.; Hennekam, Raou 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 39 KB 👁 3 views

A triad of acral, renal, and ocular abnormalities was reported previously in four families. W e report on a fifth family, in which a mother, one of her four sons and one of her two daughters are affected. Major findings in the acro-renal-ocular syndrome are upper limb abnormalities, mainly thumb hyp

Human disorganization complex, as a poly
✍ Wilmer Noé Delgado Luengo; María Luisa Hernández Rodríguez; Ivonne Valbuena Pire 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 328 KB

## Abstract We describe a baby girl of 4,000 g and 55 cm with supernumerary, malformed, and partially duplicated lower limbs, malformed and partially duplicated pelvis, spina bifida, coccygeal dermal sinus, ectopic anus located in the right buttock, duplicated internal genitalia, rectovaginal fistu