scholarly journals Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management

Cureus ◽  
2020 ◽  
Author(s):  
Chanan Goyal ◽  
Waqar Naqvi ◽  
Arti Sahu
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Male Child ◽  
Rare Case Report ◽  
Insight Into

A rare case report of corrected transposition of the great arteries in association with tuberous sclerosis and cardiac rhabdomyomas

2013 ◽  
Vol 24 (5) ◽  
pp. 955-957
Author(s):  
Rajiv Garg ◽  
Bhavesh Thakkar ◽  
Nilesh Oswal
Keyword(s):  
Case Report ◽  
Tuberous Sclerosis ◽  
Rare Case ◽  
Male Child ◽  
Rare Association ◽  
Rare Case Report ◽  
Congenitally Corrected Transposition ◽  
Corrected Transposition

AbstractThe neuro-cutaneous syndrome tuberous sclerosis is commonly associated with rhabdomyomas in various organs including the heart. We are reporting a rare case of a 7-month old male child with congenitally corrected transposition of the great arteries associated with tuberous sclerosis and cardiac rhabdomyomas. To our knowledge, this rare association has not been reported so far.

scholarly journals Dysembryoplastic neuropithelial tumor: a rare case report

2017 ◽  
Vol 5 (5) ◽  
pp. 2270
Author(s):  
Shailesh Thanvi ◽  
Hemant Jangid ◽  
Yogi Raj Joshi
Keyword(s):  
Young Adults ◽  
Case Report ◽  
Rare Case ◽  
Male Child ◽  
Adjuvant Chemoradiotherapy ◽  
Rare Entity ◽  
Intractable Seizures ◽  
Rare Case Report ◽  
Children And Young Adults ◽  
Space Occupying Lesion

Dysembryoplastic neuropithelial tumor (DNET) is a rare recently described, benign glioneural tumor frequently associated with intractable seizures in children and young adults which is important to recognise clinically and radiologically as it is surgically curable without need for adjuvant chemoradiotherapy. We hereby present a case report of a 10year old male child who presented with intractable seizures and right parietal space occupying lesion which was diagnosed DNET radiologically, treated by microsurgical excision and confirmed histopathologically as DNET, thus emphasising multidisciplinary role in management of this rare entity.

scholarly journals Rowell Syndrome in a 4-Year-Old Male Child: A Rare Case Report

2019 ◽  
Vol 3 (7) ◽  
pp. 224-226
Author(s):  
Sukhmani Brar ◽  
Jayati Batra ◽  
Balvinder Kaur Brar
Keyword(s):  
Case Report ◽  
Erythema Multiforme ◽  
Lupus Erythematosus ◽  
Rare Case ◽  
Male Child ◽  
Disease Entity ◽  
Middle Aged ◽  
Rare Case Report

Rowell syndrome is an unusual disease entity characterized by the occurrence of erythema multiforme(EM) in association with lupus erythematosus(LE). The syndrome occurs mostly in middle aged women. We are reporting this case in a 4 year old child.

Natal tooth in a seven months premature male child: A rare case report

2013 ◽  
Vol 3 (2) ◽  
pp. 182 ◽  
Author(s):  
KanikaG Verma ◽  
Pradhuman Verma ◽  
Navneet Singh ◽  
SureshK Sachdeva
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Male Child ◽  
Rare Case Report

Variant of bohring-opitz syndrome: A rare case report

2021 ◽  
Vol 4 (2) ◽  
pp. 84-86
Author(s):  
Ramesh Choudhary ◽  
Romesh Gauttam ◽  
Vishnu Pansari ◽  
Anand Kumawat
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Medical Literature ◽  
Male Child ◽  
Rare Syndrome ◽  
First Case ◽  
Eventration Of Diaphragm ◽  
Rare Case Report ◽  
Opitz Syndrome

Bohring–Opitz syndrome also known as Opitz C syndrome or Oberklaid–Danks syndrome is a rare syndrome. We are reporting a 2 months old male child with Bohring-Opitz like syndrome with all classical features and eventration of diaphragm   (left side) which has not  been reported yet with this syndrome.  To our knowledge, a total of 23 cases with this syndrome have been reported in the medical literature to date and this is probably the first case report from India. Although there is overlap, a clinical distinction from the Bohring-Opitz syndrome and other syndromes seems possible, and thus a specific causal entity may be postulated.

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report
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