Isolated Left Ventricular Apical Hypoplasia without Lamin A/C Gene Mutation
Int. j. cardiovasc. sci. (Impr.)
; 35(1): 136-139, Jan.-Feb. 2022. graf
Article
ي En
| LILACS
| ID: biblio-1356313
المكتبة المسؤولة:
BR1.1
ABSTRACT
Abstract Isolated left ventricular apical hypoplasia is a rare cardiomyopathy, with a broad range of clinical presentations. Since this entity was already described in association with osteomuscular diseases, mutation in the Lamin A/C gene has been regarded as a possible cause of this disease. This study describes the case of an asymptomatic teenager with isolated left ventricular apical hypoplasia and arthrogriposis but with no mutations in the entire Lamin A/C gene.
Key words
النص الكامل:
1
الفهرس:
LILACS
الموضوع الرئيسي:
Lamin Type A
/
Isolated Noncompaction of the Ventricular Myocardium
نوع الدراسة:
Diagnostic_studies
/
Etiology_studies
المحددات:
Adolescent
/
Humans
/
Male
اللغة:
En
مجلة:
Int. j. cardiovasc. sci. (Impr.)
موضوع المجلة:
CARDIOLOGIA
السنة:
2022
نوع:
Article