Oto-palato-digital syndrome in an Iranian infant.

Farhud DD, Walizadeh GR, Farhud I.

Department of Human Genetics and Anthropology, Amir-Kabir Hospital, Tehran
Medical Science University, Vallie Assr Sq.

A male infant is presented with wide fontanels, micrognathia, mid-face
hypoplasia, hypertelorism, broad nasal root, down-slanting palpebral fissures,
small thorax, funnel chest, short wide toes, camptodactyly and cutaneous
syndactyly of fingers and toes, dysplastic bones with thin wavy ribs and bowed
femore, cryptorchidism, and hypospadias grade I. The mother of this infant
showed some signs of the same condition, including hypertelorism, micrognathia,
small nose with depressed bridge, flat mid-face, impacted teeth and small chest.
This case shows many similarities to oto-palatal-digital syndrome types I and
II.