𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Sister and brother with Vici syndrome: Agenesis of the corpus callosum, albinism, and recurrent infections

✍ Scribed by Chiyonobu, Tomohiro ;Yoshihara, Takao ;Fukushima, Yoko ;Yamamoto, Yasutoshi ;Tsunamoto, Kentaro ;Nishimura, Yasutaka ;Ishida, Hiroyuki ;Toda, Tatsushi ;Kasubuchi, Yasuo


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
288 KB
Volume
109
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Albinism and agenesis of the corpus call
✍ del Campo, Miguel; Hall, Bryan D.; Aeby, Alec; Nassogne, Marie-Cecile; Verloes, πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 38 KB πŸ‘ 2 views

We report on two sibs and two other unrelated patients with agenesis of corpus callosum, oculocutaneous albinism, repeated infections, and cardiomyopathy. All manifested postnatal growth retardation, microcephaly, and profound developmental delay. Additional central nervous system anomalies present

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‘ 1 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