Pai syndrome: An adult patient with bifid nose and frontal hairline marker

A 17-year-old previously unreported patient with Pai syndrome is described. The boy had median cleft of upper lip, a polypoid skin mass over the columella, a minimal cleft of the upper central incisors, frontal alopecia of the anterior hairline, and bifid nose. Magnetic resonance imaging showed peri...

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Veröffentlicht in:	The Cleft palate-craniofacial journal 2003-05, Vol.40 (3), p.325-328
Hauptverfasser:	COBAN, Y. Kenan, BORAN, Cetin, OMEROGLU, S. Alp, OKUR, Erdogan
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Alopecia - complications Biological and medical sciences Brain Neoplasms - complications Cleft Lip - complications Corpus Callosum Dentistry Dermatology Humans Lipoma - complications Magnetic Resonance Imaging Male Medical sciences Nasal Polyps - complications Non tumoral diseases Nose - abnormalities Otorhinolaryngology. Stomatology Skin involvement in other diseases. Miscellaneous. General aspects Syndrome Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology
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Beschreibung
Zusammenfassung:	A 17-year-old previously unreported patient with Pai syndrome is described. The boy had median cleft of upper lip, a polypoid skin mass over the columella, a minimal cleft of the upper central incisors, frontal alopecia of the anterior hairline, and bifid nose. Magnetic resonance imaging showed pericallosal lipoma. No mental retardation was present, and a chromosomal study showed normal male 46, XY karyotype.
ISSN:	1055-6656 1545-1569
DOI:	10.1597/1545-1569(2003)040<0325:PSAAPW>2.0.CO;2