Fibulo-ulnar hypoplasia-renal anomalies syndrome https://www.malacards.org/card/fibulo_ulnar_hypoplasia_renal_anomalies_syndrome https://www.malacards.org/card/fibuloulnar_aplasia_or_hypoplasia_with_renal_abnormalities GARD:0000320 FIBULOULNAR aplasia or hypoplasia with renal abnormalities MONDO:0009233 Saito-Kuba-Tsuruta syndrome OMIM:228940 Fibulo ulnar hypoplasia renal anomalies MESH:C537226 Saito Kuba Tsuruta syndrome Orphanet:2256 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. UMLS:C1856727 MEDGEN:383972 SCTID:716094008 multiple congenital anomalies/dysmorphic syndrome without intellectual disability