## 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 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
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📜 SIMILAR VOLUMES
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
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
## 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