3C syndrome, also known as CCC dysplasia, Craniocerebellocardiac dysplasia or Ritscher Schinzel syndrome , is a rare condition.
According to several authors cranio-cerebello-cardiac (3C) syndrome is an autosomal desease.

Answered by Shweta Singh , an ibibo Advisor, at 9:40 PM on January 27, 2009

3C syndrome (medical condition) is a rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name.

Answered by Shishir , an ibibo Master, at 7:48 PM on January 09, 2009

3C syndrome, also known as CCC dysplasia, Craniocerebellocardiac dysplasia or Ritscher Schinzel syndrome, is a rare condition, characterized by cardiac malformation (heart defects), cerebellar hypoplasia and cranial dysmorphism (symptoms involving the brain). 3C syndrome is believed to follow an autosomal recessive pattern of inheritance, though the molecular basis is unknown of.Since it was first reported in 1987 by Ritscher and Schinzel[2] there has been at least 20 individuals with this condition

Answered by Deepak , an ibibo Advisor, at 2:46 PM on January 09, 2009