scholarly journals RARE ASSOCIATION OF CELIAC DISEASE WITH CONGENITAL HEART DISEASE

2019 ◽  
Vol 6 (5) ◽  
pp. 255-256
Author(s):  
Rashi Bhargava ◽  
Aaradhana Singh ◽  
Anju Aggarwal ◽  
Manish Narang
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Celiac Disease ◽  
Congenital Heart ◽  
Rare Association

scholarly journals RARE ASSOCIATION OF CELIAC DISEASE WITH CONGENITAL HEART DISEASE

2019 ◽  
Vol 6 (5) ◽  
pp. 255-256
Author(s):  
Rashi Bhargava ◽  
Aaradhana Singh ◽  
Anju Aggarwal ◽  
Manish Narang
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Celiac Disease ◽  
Congenital Heart ◽  
Rare Association

Rectal atresia, choanal atresia and congenital heart disease: A rare association

2004 ◽  
Vol 12 (4) ◽  
pp. 343-345 ◽  
Author(s):  
A.K. Saxena ◽  
J.J. Morcate ◽  
J. Schleef ◽  
A. Reich ◽  
G.H. Willital
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Congenital Heart ◽  
Choanal Atresia ◽  
Rare Association ◽  
Rectal Atresia

scholarly journals RARE ASSOCIATION OF DOWN SYNDROME WITH DANDY WALKER MALFORMATION

2014 ◽  
Vol 04 (02) ◽  
pp. 140-141
Author(s):  
Suresh Goyal ◽  
Vignesh Nayak H. ◽  
Reeta Meena
Keyword(s):  
Congenital Heart Disease ◽  
Down Syndrome ◽  
Heart Disease ◽  
Congenital Heart ◽  
Rare Association ◽  
Dandy Walker Malformation ◽  
Walker Malformation ◽  
Systemic Condition

Abstract:We report on a patient with Down syndrome and a multi-systemic condition comprising congenital heart disease (ASD) and neurological malformation (Dandy walker malformation). The co-occurrence of Down syndrome (DS) and Dandy walker malformation is relatively uncommon

scholarly journals A rare association of incontinentia pigmenti with congenital heart disease in a newborn

2021 ◽  
Vol 22 (4) ◽  
pp. 342
Author(s):  
Mounica Chimbili ◽  
AshaGowrappala Shanmukhappa ◽  
Leelavathy Budamakuntla ◽  
Shilpa Kanathur
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Congenital Heart ◽  
Incontinentia Pigmenti ◽  
Rare Association

scholarly journals Tracheal Stenosis and Congenital Heart Disease in Trisomy 21

Children ◽  
2019 ◽  
Vol 6 (9) ◽  
pp. 98
Author(s):  
Kylat
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Tracheal Stenosis ◽  
Trisomy 21 ◽  
Congenital Heart ◽  
Upper Airway ◽  
Chromosomal Anomalies ◽  
Rare Association ◽  
Wide Range ◽  
Airway Anomalies

Tracheal rings (TR) are rare, congenital cartilaginous defect of the upper airway and are usually due to complete or near complete circumferential cartilaginous tracheal rings, with variable degrees of tracheal stenosis (TS) and shortening. Chromosomal anomalies like trisomy 21 are characteristically associated with a wide range of upper airway anomalies including TS and congenital heart disease (CHD). However, the overall prevalence of severe forms of TS is rare and reported in 1.2% of all CHD patients. Herein, we present a rare association of severe TS due to complete tracheal rings in a trisomy 21 patient with CHD and the challenges in the management.

scholarly journals Trisomy 21 and Ebstein Anomaly: Diagnosis and Prognosis of a Rare Association

2020 ◽  
Author(s):  
Gabriela Rangel Brandão ◽  
Amanda Thum Welter ◽  
Gabriel Dotta Abech ◽  
Carla Bastos da Costa Almeida ◽  
Caio Seiti Mestre Okabayashi ◽  
...  
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Literature Review ◽  
Tricuspid Valve ◽  
Trisomy 21 ◽  
Congenital Heart ◽  
Good Prognosis ◽  
Ebstein Anomaly ◽  
Rare Association ◽  
Diagnosis And Prognosis

AbstractTrisomy 21 is considered the most common chromosomal aneuploidy, and congenital heart disease (CHD) is highly prevalent and relevant to the morbidity and mortality of these patients. Ebstein anomaly (EA) is a rare CHD characterized by tricuspid valve dysplasia with inferior septal leaflet displacement. Herein, we describe a patient with trisomy 21 who presented with EA and discuss the association between the two conditions based on a literature review. We conclude that the concomitant occurrence of both conditions is considered to be rare. These individuals are most frequently diagnosed during birth and childhood, and they usually have a good prognosis, as observed with our patient and is typical for EA patients in general. However, it is important to be aware that electrophysiologic anomalies may also be present.

scholarly journals Rare Association of Congenital Facial Palsy, Bilateral Microtia and Congenital Heart Disease

2018 ◽  
Vol 37 (2) ◽  
pp. 201-203
Author(s):  
Aditi Rawat ◽  
Dipika Bhil ◽  
Bakul B Javadekar
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Facial Palsy ◽  
Congenital Heart ◽  
Female Child ◽  
Gray Zone ◽  
Renal Ectopia ◽  
Rare Association ◽  
Depressor Anguli Oris

We report a case of a two day old female child with congenital facial palsy, bilateral microtia, congenital heart disease, renal ectopia and unilateral hypoplasia of depressor anguli oris muscle. These constellation of symptoms have not been found together in any case before. This unknown syndrome could be considered to be in a gray zone between Caylers Cardiofacial syndrome and Pearls syndrome.

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