Catalog

Frank-ter Haar syndrome

No MMS code

Link to WHO Definition

Frank-ter Haar syndrome – http://id.who.int/icd/entity/1643548765

Frank-ter Haar syndrome (formerly considered as an autosomal recessive form of Melnick-Needles syndrome) is defined by the association of megalocornea, multiple skeletal anomalies, characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism, prominent eyes, full cheeks and micrognathia) and developmental delay.