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Camurati-Engelmann disease in a family from Croatian Island: an old bone scan confirmed pattern of inheritance.

Collegium antropologicum - 1 Jun 2014

Baretić Maja, Korsić Mirko, Potocki Kristina, Horvatić Gordana Herceg, Orlić Zeljka Crncević

Abstract excerpt

34-year old patient had history of muscular wasting, easy fatigability, pain in extremities and waddling gait since age of four. During the time, neuromuscular disease was suspected, but not confirmed. Elevated bone alkaline phosphatase as well as other bone turnover markers (osteocalcin, procollagen, telopeptide) indicated further skeletal evaluation. Symmetrical enhanced uptake on technetium methylene...

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PMID: 25145018

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