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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease craniofacial microsomia
Comorbidity C0265264|holt-oram syndrome
Sentences 1
PubMedID- 21184723 This is an unusual case of a patient with holt-oram syndrome associated with facial anomalies: hemifacial microsomia on the right side, forehead prominent and tall, hypertelorism, depressed nasal bridge, low set ears and micrognathia.

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