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Caudal deficiency and asplenia anomalies in sibs
A Fullana1, E Garcia-Frias, M L Martinez-Frias
1Servicio de Neonatología, Clínica Infantil, La Paz, Facultad de Medicina, Universidad Autónoma de Madrid, Spain.
American Journal of Medical Genetics. Supplement
|January 1, 1986
Abstract:
The caudal deficiency and asplenia anomalies have been described separately in children. Two sibs with these two entities are described. Only another similar case, with caudal deficiency and polysplenia anomalies was found in the literature. It is possible that this association could be a new syndromic entity. An autosomal recessive mode of inheritance is suggested.