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We report a Bedouin family with gerodermia osteodysplasiea in which there are two affected female siblings. They have a prematurely aged face with loose and wrinkled skin, joint laxity/dislocation, and osteoporosis. Unusual traits that nave not been previously reported in association with gerodermia osteodysplastica were ear anomalies and an abnormal EEG.
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Al‐Torki et al. (1997) studied this question.
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