Multiple exostoses
Hereditary disorder transmitted by autosomal dominant genes (EXT1-3) and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation.
Disease Alternative Name
Recent Cases of Multiple exostoses
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Top doctors who continously share their opinions on Multiple exostosesSuper Specialist in Reproductive Endocrinology

Fortis Anandapur
Clinical Associate/Assoc Consult
Peerless Hospital and B.K Roy Research Centre
DNB Orthopaedic Surgery, IMRCS

Krishna Institute of Medical Sciences (KIMS)
Chief Geneticist
Center of Medical Genetics, Sir Ganga Ram Hospital
PhD Human Genetics


Sunshine Hospitals
Consultant Joint Replacement Surgeon
Kamineni Hospitals
DNB in Orthopaedics

Trending Cases
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Dr. Nirmal Shah0 Like1 AnswerA female 36 years, gravida 3 para 2 comes with complaints of headache, loss of sight and is in labour with poor cervical dilatation progress. on admission, the BP is 178/102 with no history of convulsions and magnesium sulphate is given. A LSCS is performed under spinal anesthesia with BP stabilised. she is transferred to ICU for post operative management with BP continuing to increase . After 5 days, a feedback is given that the patient is discharged and gained her sight. What caused the loss of sight?
Dr. Prashant Vedwan1 Like0 Answer
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