Antley-Bixler syndrome in sisters: A term newborn and a prenatally diagnosed fetus
β Scribed by Schinzel, Albert ;Savoldelli, Guido ;Briner, Jakob ;Sigg, Peter ;Massini, Carlo ;Opitz, John M.
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 519 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0148-7299
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Oral-facial-digital syndrome type II (OFP syndrome II; orofaciodigital syndrome II) is a rare autosomal recessive syndrome, first described by Mohr (1941). We present two sisters with Mohr syndrome from a consanguineous family. One is a three-day-old female patient, the other is 22-week-old fetus. P
We describe two sib fetuses with situs inversus, cystic dysplastic kidney and pancreas, bowing of the lower limbs and clavicles, severe intrauterine growth retardation (IUGR), and oligohydramnios. Early prenatal diagnosis of pancreatic and dysplastic renal cysts and situs inversus totalis were made