Oral-facial-digital syndrome, Type I: A case report

2003 ◽  
Vol 26 (2) ◽  
pp. 211-215 ◽  
Author(s):  
N. King ◽  
A. Sanares
Keyword(s):  
Case Report ◽  
Congenital Anomalies ◽  
Type I ◽  
Syndrome Type ◽  
Dominant Trait ◽  
Southern Chinese ◽  
Chinese Girl ◽  
The Face ◽  
Mandibular Canine

Oral-facial-digital syndrome is a group of congenital anomalies, which affects the face, oral structures and digits. There are nine subtypes. OFDS type I, is x-linked dominant trait mostly affecting females. Reports of OFDS type 1 in Asians are extremely rare. This paper shows a case of OFDS type I, in a southern Chinese girl, who in addition to most of the classic features, had fusion of the mandibular canine and lateral incisor teeth.

scholarly journals Oral-Facial-Digital Syndrome Type 1: Oral Findings in a 6-Year-Old Girl

2018 ◽  
Vol 07 (02) ◽  
pp. 092-096
Author(s):  
Zuhal Kırzıoglu ◽  
Esra Oz
Keyword(s):  
Oral Cavity ◽  
X Chromosome ◽  
Congenital Anomalies ◽  
Syndrome Type ◽  
Developmental Genetic ◽  
The Face ◽  
Genetic Anomaly

AbstractOral-facial-digital syndrome (OFDS) is a group of congenital anomalies with 13 different forms. OFDS type 1 (OFDS1) is a developmental genetic anomaly related to the X chromosome, that is often seen in girls, and affects the face, oral cavity, and extremities. In this study, we discuss the oral findings of a 6-year-old girl with OFDS1 and her situation after 2.5 years.

scholarly journals Branchial fistula: review of literature and case report

2017 ◽  
Vol 4 (11) ◽  
pp. 3576
Author(s):  
Salil Mahajan ◽  
Jaya Sorout
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Congenital Anomalies ◽  
Type I ◽  
Review Of Literature ◽  
Radiological Findings ◽  
Congenital Lesions ◽  
Branchial Arches ◽  
The Face ◽  
Branchial Fistula

The branchial arches are the embryological precursors of the face, neck and pharynx. Second most common congenital lesions of the head and neck in children are the anomalies of the branchial arches, with second arch anomalies by far the most common. Clinically, these congenital anomalies may present as cysts, sinus tracts, fistulae or cartilaginous remnants with typical clinical and radiological findings. We report the case of 11-month-old male child with congenital Type I Second branchial fistula on the left side of neck.

Management of Complex Regional Pain Syndrome Type 1 with Barbiturate Coma Therapy -A case report-

2006 ◽  
Vol 19 (2) ◽  
pp. 213
Author(s):  
Tae Kyu Park ◽  
Kyung Ream Han ◽  
Dong Wook Shin ◽  
Young Joo Lee ◽  
Chan Kim
Keyword(s):  
Case Report ◽  
Complex Regional Pain Syndrome ◽  
Pain Syndrome ◽  
Syndrome Type ◽  
Barbiturate Coma

scholarly journals Waardenburg’s Syndrome (Type 1) in A Newborn of Consanguineous Parents: A Case Report

2015 ◽  
Vol 38 (3) ◽  
pp. 157-160
Author(s):  
Sharifun Naher ◽  
Animesh Chandra Das
Keyword(s):  
Case Report ◽  
Child Health ◽  
Syndrome Type

Abstract not available DOI: http://dx.doi.org/10.3329/bjch.v38i3.22825 Bangladesh J Child Health 2014; VOL 38 (3) :157-160

scholarly journals An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature

2018 ◽  
Vol 44 (1) ◽  
Author(s):  
Giulia Trippella ◽  
Paolo Lionetti ◽  
Sara Naldini ◽  
Francesca Peluso ◽  
Matteo Della Monica ◽  
...  
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Syndrome Type ◽  
Review Of Literature ◽  
Trichorhinophalangeal Syndrome ◽  
Trichorhinophalangeal Syndrome Type 1

Bilateral duane’s syndrome Type I in siblings: Case Report

2020 ◽  
pp. 271-275
Author(s):  
C. Schiavi ◽  
M. Fresina ◽  
F. Quagliano ◽  
E.C. Campos
Keyword(s):  
Case Report ◽  
Type I ◽  
Syndrome Type ◽  
Duane’S Syndrome
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