Ulbright-Hodes syndrome

Ulbright-Hodes syndrome is characterized by renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a potter-like facies. The syndrome has been described in three infants (one pair of sibs and an unrelated case), all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive.

Also known as: renal dysplasia-limb defects syndrome, renal dysplasia-mesomelia-radiohumeral fusion syndrome, RL syndrome, Ulbright Hodes syndrome, renal dysplasia limb defects syndrome, renal dysplasia, mesomelia, and radiohumeral fusion

0 clinical trials for this condition and its sub-types, 0 tagged with Ulbright-Hodes syndrome itself.