scholarly journals Lipoma of Columella with septal extension in Pai syndrome: report of a rare case

2017 ◽  
Vol 17 (1) ◽  
Author(s):  
Surendra B. Patil ◽  
Shree Harsh
Keyword(s):  
Rare Case ◽  
Syndrome Report

The prune belly syndrome: report of a rare case and review of literature

2011 ◽  
Vol 35 (3) ◽  
pp. 241-243 ◽  
Author(s):  
Kristoff Verdonck ◽  
Gregory Van Eeckhout ◽  
Veerle De Boe ◽  
Paul Wylock
Keyword(s):  
Rare Case ◽  
Prune Belly Syndrome ◽  
Review Of Literature ◽  
Prune Belly ◽  
Syndrome Report

scholarly journals Adult grisel’s syndrome: report of a rare case

2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Alfredo Carvalho ◽  
André Pinho ◽  
Francisco Serdoura ◽  
Vitorino Veludo
Keyword(s):  
Rare Case ◽  
Grisel’S Syndrome ◽  
Syndrome Report

CEDNIK Syndrome: Report of an Ultra-Rare Case from India

2021 ◽  
Vol 69 (6) ◽  
pp. 1861
Author(s):  
ParagM Tamhankar ◽  
Vandana Bansal ◽  
VasundharaP Tamhankar ◽  
ShilpaM Mithbawkar
Keyword(s):  
Rare Case ◽  
Syndrome Report

scholarly journals Rectal Villous Adenoma with McKittrick-Wheelock Syndrome: Report of a Rare Case

2013 ◽  
Vol 29 (1) ◽  
pp. 55-58 ◽  
Author(s):  
Yu-Hung Chen ◽  
Jung-Cheng Kang ◽  
Huang-Jen Lai
Keyword(s):  
Villous Adenoma ◽  
Rare Case ◽  
Rectal Villous Adenoma ◽  
Syndrome Report

Oral and Dental Manifestations in Rubinstein-Taybi Syndrome: Report of a Rare Case

2012 ◽  
Vol os19 (1) ◽  
pp. 35-38 ◽  
Author(s):  
Madiraju Gunashekhar ◽  
Mohammad Shahul Hameed ◽  
Syed Kamran Bokhari
Keyword(s):  
Rare Case ◽  
Autosomal Dominant ◽  
Postnatal Growth ◽  
Dominant Inheritance ◽  
Supernumerary Tooth ◽  
Growth Deficiency ◽  
Craniofacial Dysmorphism ◽  
Rare Congenital Disorder ◽  
Broad Thumbs ◽  
Syndrome Report

Rubinstein-Taybi syndrome, or broad thumb-hallux syndrome, is a well-defined rare congenital disorder characterised by postnatal growth deficiency, craniofacial dysmorphism, broad thumbs and great toes, and mental retardation (intellectual disability). Occurrence may be either sporadic or through autosomal dominant inheritance. Reports of Rubinstein-Taybi syndrome are scarce in the literature. This case report describes the oral and dentofacial findings of Rubinstein-Taybi syndrome affecting a 13-year-old Indian female, including the uncommon presence of talon cusps and an unerupted supernumerary tooth.

scholarly journals Woakes’ syndrome: Report of a rare case

2019 ◽  
Vol 5 (3) ◽  
pp. 062-064
Author(s):  
T Shi Nee ◽  
A Hazwan ◽  
Hamzah SZ Syed
Keyword(s):  
Rare Case ◽  
Syndrome Report

scholarly journals Jaffe-Lichtenstein syndrome - Report of a rare case

2019 ◽  
Vol 4 (4) ◽  
pp. 194-197
Author(s):  
Shaul Hameed. K ◽  
Laxmikant Chatra ◽  
Prasanth Shenoy ◽  
Anoop Kurian Mathew
Keyword(s):  
Rare Case ◽  
Syndrome Report

scholarly journals Apert′s syndrome: Report of a rare case

2013 ◽  
Vol 17 (2) ◽  
pp. 294 ◽  
Author(s):  
PurvS Patel ◽  
YeshaV Jani ◽  
NareshC Soni ◽  
ParulV Bhatia
Keyword(s):  
Rare Case ◽  
Syndrome Report
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