LAURENCE MOON BIEDYL SYNDROME: A RARE CASE REPORT
Udayalakshmi K.*, Bhavya V., Hemalata A., Lakshmi P. and Dr. Ranganayakulu D.
ABSTRACT
Laurence moon Biedyl syndrome is a rare autosomal recessive condition with a wide spectrum of clinicalfeatures. The accepted major criteria for diagnosis include retinal dystrophy, obesity, Polydactyly, male hypogonadism, mental retardation and renal dysfunction. We have presented a 36 year old male patient exhibiting characteristic features of Laurence moon Biedyl syndrome and then the literature is reviewed.
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