Papillon-Leage and psaume syndrome patient with multiple dental and orofacial anomalies

Yükleniyor...
Küçük Resim

Tarih

2019

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Wolters Kluwer Medknow Publications

Erişim Hakkı

info:eu-repo/semantics/embargoedAccess

Özet

Papillon-Leage-Psaume Syndrome, also known as oral-facial-digital syndrome (OFDS) type I, describes a group of neurodevelopmental disorders that are characterized by anomalies of the oral cavity, facial features, and the digits. Central nervous system (CNS) anomalies and visceral organ abnormalities such as kidney, pancreas, and ovarian cysts can also be seen in these patients. Among 13 potential types, female-inherited OFDS type I is the most common and it has been reported to be lethal in males. After the identification of the genetic relation of OFDS in 2001, it is now known that, except X-linked OFDS Type I and VIII, generally all types of OFDSs are autosomal recessive. The dentist's knowledge about the syndrome can reduce the development of physical and dental anomalies by facilitating early diagnosis. This article presents a patient with Papillon-Leage-Psaume Syndrome (Oral-Facial-Digital Syndrome Type I).

Açıklama

WOS: 000471973600021
PubMed ID: 31187776

Anahtar Kelimeler

Cleft Palate, Oral-Facial-Digital Syndrome Type I, Papillon-Leage Psaume Syndrome

Kaynak

Nigerian Journal of Clinical Practice

WoS Q Değeri

Q4

Scopus Q Değeri

Q3

Cilt

22

Sayı

6

Künye

Kılınç, D. D. ve Özsarp, E. (2019). Papillon-Leage and psaume syndrome patient with multiple dental and orofacial anomalies. Nigerian Journal of Clinical Practice, 22(6), 872-876. https://dx.doi.org/10.4103/njcp.njcp_451_18