## Abstract Holoprosencephaly (HPE) and craniosynostosis are separate conditions that have occasionally been observed to occur simultaneously in the same patient. Here, we compile patients with both conditions who have been documented in the literature thus far; moreover, we report on two additiona
The Richieri-Costa and Pereira syndrome: Report of two Brazilian siblings and review of literature
✍ Scribed by Josiane Souza; Karin dal Vesco; Rita Tonocchi; Maria Cecília Closs-Ono; Maria Rita Passos-Bueno; Renato da Silva-Freitas
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 155 KB
- Volume
- 155
- Category
- Article
- ISSN
- 1552-4825
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We report on a French boy with cleft mandible, pre/postaxial hand anomalies, and clubfoot born to consanguineous parents. These findings are comparable to those of previous cases of the autosomal recessive Richieri-Costa and Pereira syndrome of short stature, Robin sequence, cleft mandible, pre/post
T w o Japanese sibs with the Meckel syndrome are reported. Both babies showed the classical triad of this condition: occipital encephalocele, cystic kidneys, and postaxial polydactyly of all four limbs. The diagnostic criteria and differential diagnosis were reviewed.
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