Case report highlights unique features of Poland-Möbius syndrome, suggesting a need for better understanding.
The Poland‐Möbius syndrome is a combination of two rare congenital syndromes with an estimated prevalence of 1:500 000. It is characterized by a nonprogressive bilateral facial paralysis, the inability of the eyes to abduct beyond the midline, orofacial anomalies, limb deficiencies, and an absence or hypoplasia of the pectoral muscles.
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Maino et al. (1989) studied this question.
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