Grebe Syndrome

ACHONDROGENESIS, BRAZILIANGREBE CHONDRODYSPLASIA GREBE DYSPLASIA ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG ACHONDROGENESIS, TYPE II. Phenotype Gene Relationships OMIM NUMBER -200700 Inheritance- Autosomal Recessive. Gene map locus -20q11.2 We are reporting a rare case of GREBE SYNDROME, referred to our genetic clinic from the Department of Paediatrics, Chinglepet Medical college Hospital.So far in the world only around 700 cases have been reported.