𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Atypical findings in three patients with Pai syndrome and literature review

✍ Scribed by Damien Lederer; Brian Wilson; Pierre Lefesvre; Vincent Vander Poorten; Nigel Kirkham; Dipayan Mitra; Christine Verellen-Dumoulin; Koenraad Devriendt


Book ID
115549417
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
212 KB
Volume
158A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Pai syndrome: First patient with agenesi
✍ Marco Castori; Rosanna Rinaldi; Aurelia Bianchi; Aurelio Caponetti; Marcello Ass πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 178 KB πŸ‘ 2 views

## 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

Atypical findings in Kabuki syndrome: Re
✍ D. GeneviΓ¨ve; J. Amiel; G. Viot; M. Le Merrer; D. Sanlaville; A. Urtizberea; M. πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 134 KB πŸ‘ 2 views

## Abstract Kabuki syndrome (KS) is a rare multiple congenital anomaly/mental retardation syndrome with an estimated frequency of 1/32,000 in Japan. Five major criteria delineate KS namely postnatal short stature, skeletal anomalies, moderate mental retardation, dermatoglyphic anomalies, and a char