Cornelia de lange syndrome
A rare syndrome characterized by low birth weight, delayed growth, mental retardation, behavioral problems, and a distinctive facial appearance (thin, arched eyebrows, low set ears, small teeth, and small nose). The majority of cases are caused by mutations in the NIPBL gene. Less severe forms of the syndrome are caused by mutations in the SMC1A and SMC3 genes.
Recent Cases of Cornelia de lange syndrome
Browse recently discussed Cornelia de lange syndrome cases by specialistsTop Cornelia de lange syndrome Doctors on Curofy
Top doctors who continously share their opinions on Cornelia de lange syndromeGandhi Medical College.
M.B.B.S.

BHASKARA HOSPITAL
OBSTETRICIAN &GYNECOLOGIST
Kakatiya Medical College
M.D ( OB&GY )




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