## Abstract The short rib‐polydactyly (SRP) group are lethal skeletal dysplasias with an autosomal recessive inheritance pattern that can be distinguished on radiological and histological grounds. We report on two consecutive pregnancies complicated by a SRP syndrome with acromesomelic hypominerali
✦ LIBER ✦
Diagnostic dilemmas in the short rib-polydactyly syndrome group
✍ Scribed by Elçioglu, Nursel H. ;Hall, Christine M.
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 294 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0148-7299
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Up to seven short-rib-polydactyly (SRP) syndromes have been identified so far with marked clinical and pathological overlap. We describe a 32-week-old, nonhydropic male fetus with thoracic ''dysplasia,'' short limbs, and unilateral postaxial polydactyly. All internal organs were normally developed,