Diaphyseal aclasis

An autosomal dominant skeletal disorder caused by mutations in the TGFB1 gene. It is characterized by thickening of the bones, particularly the long bones of the extremities. It is associated with muscle weakness and tiredness.

Disease Alternative Name

camurati-engelmann syndrome
progressive diaphyseal dysplasia
camurati-englemann disease
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Burla.Odisha
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Patna Medical College.

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GOVT MEDICAL COLLEGE Kottayam

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Karimnagar
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Chelmeda Anand Rao Institute of Medical Sciences Bommakal

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KAMINENI INSTITUTE OF MEDICAL SCIENCES

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Surat
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Trivandrum
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Trivandaram Medical College

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Surabhi Institute of Medical Sciences

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Sunshine Hospital

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