Hydrocephaly - tall stature - joint laxity is a multiple congenital anomalies syndrome described in two sisters and characterized by the presence of hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis. There have been no further descriptions in the literature since 1989. The disease is Orphanet rare-disease nomenclature entry Orphanet_2181 (Hydrocephaly - tall stature - joint laxity). Also known as: Daish-Hardman-Lamont syndrome.