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“C” Trigonocephaly syndrome: Report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and review

✍ Scribed by Glickstein, Julie ;Karasik, Jeffrey ;Caride, Diana Garcia ;Marion, Robert W.

Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
437 KB
Volume
56
Category
Article
ISSN
0148-7299

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## Abstract ## BACKGROUND: Pai syndrome (PS) is a rare regional developmental defect of the face, mainly characterized by the variable association of midline cleft of the upper lip (MCL), duplicated maxillary median frenulum, and midline facial cutaneous and midanterior alveolar process polyps. It