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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Bibliographic Details
Published in:The Cleft palate-craniofacial journal 2003-05, Vol.40 (3), p.325-328
Main Authors: COBAN, Y. Kenan, BORAN, Cetin, OMEROGLU, S. Alp, OKUR, Erdogan
Format: Article
Language:English
Subjects:
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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Description
Summary: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