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Figure 2 | Cases Journal

Figure 2

From: Oculopharyngeal muscular dystrophy as a rare differential diagnosis for unexplained dysphagia: a case report

Figure 2

Pedigree of the patient (marked by arrow) indicating autosomal-dominant transmission of OPMD. One 69 year old brother (marked by a question mark) of the index patient was reported to have only mild dysphagia without eyelid ptosis which may reflect mild expression of the disease or even chance association. The affection status of the paternal grandmother (marked by a question mark) is unclear because she died already at the age of 36 years.

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