Literature DB >> 18657395

Phenotypic variability of Pai syndrome: report of two patients and review of the literature.

F Vaccarella1, A Pini Prato, A Fasciolo, M Pisano, C Carlini, P L Seymandi.   

Abstract

Pai syndrome is a rare form of frontonasal dysplasia, first described in 1987. It is a triad consisting of midline cleft of the upper lip, facial skin polyps and central nervous system lipomas. Only 14 cases have been reported in the literature. The authors describe the clinical features, diagnostic workup and treatment of two patients. A review of all cases reported in literature is presented to show the phenotypic variability of this rare syndrome.

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Year:  2008        PMID: 18657395     DOI: 10.1016/j.ijom.2008.06.007

Source DB:  PubMed          Journal:  Int J Oral Maxillofac Surg        ISSN: 0901-5027            Impact factor:   2.789


  4 in total

Review 1.  Pai syndrome: first reported case in Qatar and review of literature of previously published cases.

Authors:  Mohamed Abdelmaaboud; Nuha Nimeri
Journal:  BMJ Case Rep       Date:  2012-08-21

Review 2.  Pai syndrome: a review.

Authors:  Francesca Olivero; Thomas Foiadelli; Sabino Luzzi; Gian Luigi Marseglia; Salvatore Savasta
Journal:  Childs Nerv Syst       Date:  2020-07-10       Impact factor: 1.475

3.  Pai syndrome: From the womb until 19 months of age, a neurological development success story.

Authors:  Hala Hassan; Daniella L Buzas; Anne Bazin; Noëlle Stempfle; Agnès Guët; Christophe Poncelet; Cergika Veluppillai
Journal:  Clin Case Rep       Date:  2021-07-21

4.  Fibrolipoma of the nasal septum; report of the first case.

Authors:  Murat Ozturk; Kadri Ila; Ahmet Kara; Mete Iseri
Journal:  J Otolaryngol Head Neck Surg       Date:  2013-02-02
  4 in total

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