3C syndrome [cranio-cerebello-cardiac dysplasia] or ritscher schinzel syndrome: a rare case report with review of literature

ABSTRACT

A very rare case of 3C [cranio-cerebello-cardiac] inheritance of this condition due to consanguinity syndrome is reported for the first time in an Arab infant between the parents. Need of antenatal diagnosis and from Kuwait. The diagnostic features and differential genetic counseling is highlighted for this prognostically diagnosis is discussed. We support the autosomal recessive poor condition.