Roberts syndrome


Rob·erts syn·drome

(rob'ĕrtz), [MIM*268300] phocomelia or lesser degrees of hypomelia, microbrachycephaly, midfacial defect, prenatal growth deficiency, and cryptorchidism; associated with chromosomal centromeric abnormalities; autosomal recessive inheritance.

Roberts,

John B., U.S. physician, 1852-1924. Roberts syndrome - autosomal recessive inheritance, with multiple defects.

Rob·erts syn·drome

(rob'ĕrts sindrōm) [MIM*268300] Phocomelia or lesser degrees of hypomelia, microbrachycephaly, midfacial defect, prenatal growth deficiency, and cryptorchidism.