Johnson neuroectodermal syndrome is characterized by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism.
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Neu-Laxova syndrome
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acrofacial dysostosis, Catania type
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ADULT syndrome
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autosomal dominant palmoplantar keratoderma and congenital alopecia
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ameloonychohypohidrotic syndrome
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ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
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