Case report in Peru infant with cleft lip superior, double bridle, and columella hamartoma previous alveolar ridge (Pai Syndrome)

Authors

  • Bertha Gallardo Jugo
  • Hugo Abarca Barriga
  • Jessica Chirinos Saire

DOI:

https://doi.org/10.61651/rped.2010v63n1p39-41

Abstract

Pai syndrome is a rare congenital disorder, first described in 1987. The main clinical features of the syndrome include cleft lip medial superior, intracranial lipomas and cutaneous polyps. Until July 2008, 16 cases have been reported worldwide, seven of them in South America.

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Author Biographies

Bertha Gallardo Jugo

Genetista Pediatra del Instituto Nacional de Salud del Niño. Lima, Perú.

Hugo Abarca Barriga

Médico Genetista del Instituto Nacional de Salud del Niño. Lima, Perú.

Jessica Chirinos Saire

Médico Pediatra. Lima, Perú.

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Published

2010-12-31

How to Cite

1.
Gallardo Jugo B, Abarca Barriga H, Chirinos Saire J. Case report in Peru infant with cleft lip superior, double bridle, and columella hamartoma previous alveolar ridge (Pai Syndrome). Rev Peru Pediatr [Internet]. 2010 Dec. 31 [cited 2024 Nov. 23];63(1):39-41. Available from: https://pediatria.pe/index.php/pedperu/article/view/471

Issue

Vol. 63 Num. 1 (2010)

Section

CLINICAL CASE

Categories

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