Fibulo-ulnar hypoplasia-renal anomalies syndrome FIBULOULNAR aplasia or hypoplasia with renal abnormalities Fibulo ulnar hypoplasia renal anomalies Fibulo-ulnar hypoplasia-renal anomalies syndrome is characterized by fibuloulnar dysostosis with renal anomalies. It has been described in two sibs born to nonconsanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial anomalies (including micrognathia), symmetrical shortness of long bones, fibular agenesis and hypoplastic ulna, oligosyndactyly, congenital heart defects, and cystic or hypoplastic kidney. It is transmitted as an autosomal recessive trait. GARD:0000320 ICD10:Q87.8 MESH:C537226 MONDO:0009233 OMIM:228940 Orphanet:2256 SCTID:716094008 Saito Kuba Tsuruta syndrome Saito-Kuba-Tsuruta syndrome UMLS:C1856727 syndromic renal or urinary tract malformation genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability