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

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.

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Severe subvalvular pulmonic stenosis due to a ball-shaped accessory tissue in an asymptomatic woman with congenitally corrected transposition of great arteries and mesocardia: A rare case report

Echocardiography ◽

10.1111/echo.13751 ◽

2017 ◽

Vol 35 (1) ◽

pp. 114-117

Author(s):

Maryam Nabati ◽

Mozhdeh Dabirian

Keyword(s):

Case Report ◽

Rare Case ◽

Transposition Of Great Arteries ◽

Asymptomatic Woman ◽

Pulmonic Stenosis ◽

Rare Case Report ◽

Congenitally Corrected Transposition ◽

Corrected Transposition

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A rare case report: tricuspid valve prolapse due to spontaneous chordae rupture in a congenitally corrected transposition of the great arteries patient

Journal of Cardiothoracic Surgery ◽

10.1186/s13019-020-01193-0 ◽

2020 ◽

Vol 15 (1) ◽

Author(s):

Wan Yu Hu ◽

Bo Wen Zhao ◽

Shi Yan Li ◽

Bei Wang

Keyword(s):

Case Report ◽

Tricuspid Valve ◽

Rare Case ◽

Rare Case Report ◽

Congenitally Corrected Transposition ◽

Corrected Transposition

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Initial presentation with dilated cardiomyopathy in a patient of tuberous sclerosis: A rare case report

Indian Heart Journal ◽

10.1016/j.ihj.2012.12.012 ◽

2013 ◽

Vol 65 (1) ◽

pp. 84-87 ◽

Cited By ~ 1

Author(s):

Dharmendra Jain ◽

Vikas Kumar ◽

Deba P. Kar ◽

Shashi R. Prasad

Keyword(s):

Case Report ◽

Dilated Cardiomyopathy ◽

Tuberous Sclerosis ◽

Rare Case ◽

Initial Presentation ◽

Rare Case Report

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Dysembryoplastic neuropithelial tumor: a rare case report

International Journal of Research in Medical Sciences ◽

10.18203/2320-6012.ijrms20171887 ◽

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.

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

International Healthcare Research Journal ◽

10.26440/ihrj/0307.10294 ◽

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.

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Spigelian Hernia in 2-Year-Old Male Child: A Rare Case Report

Juniper Online Journal of Case Studies ◽

10.19080/jojcs.2017.03.555612 ◽

2017 ◽

Vol 3 (3) ◽

Author(s):

Shubhangi Sharma

Keyword(s):

Case Report ◽

Rare Case ◽

Male Child ◽

Spigelian Hernia ◽

Rare Case Report

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

Archives of International Surgery ◽

10.4103/2278-9596.122982 ◽

2013 ◽

Vol 3 (2) ◽

pp. 182 ◽

Cited By ~ 3

Author(s):

KanikaG Verma ◽

Pradhuman Verma ◽

Navneet Singh ◽

SureshK Sachdeva

Keyword(s):

Case Report ◽

Rare Case ◽

Male Child ◽

Rare Case Report

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Variant of bohring-opitz syndrome: A rare case report

IP Journal of Paediatrics and Nursing Science ◽

10.18231/j.ijpns.2021.017 ◽

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.

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