Catalog

McDonough syndrome

No MMS code

Link to WHO Definition

McDonough syndrome – http://id.who.int/icd/entity/1349711155

McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation (MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart defect.

Parents

LD2F.1 Syndromes with multiple structural anomalies, not of environmental origin
Syndromic conditions with disorders of intellectual development as a relevant clinical feature