Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism Latest Advances

Repair of Ventricular Septal Defect in Children with TAB2 Gene Anomalies and Associated Cardiomyopathy.

Journal: Surgical case reports

Published: February 09, 2026

Progeroid features in a patient with Malouf syndrome due to a rare LMNA variant: a case report and review of the literature.

Journal: Archives of endocrinology and metabolism

Published: July 24, 2025

The Quiet Burden of Iron: A Rare Case of Hereditary Hemochromatosis in Pakistan.

Journal: Cureus

Published: July 19, 2025

Testosterone in Duchenne muscular dystrophy: effects on puberty and growth.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: June 11, 2025

Possible consequences of the abuse of anabolic steroids on different organs of athletes.

Journal: Archives of physiology and biochemistry

Published: February 03, 2025

Frequency of Delayed Puberty in Boys with Contemporary Management of Duchenne Muscular Dystrophy

Journal: Journal of clinical research in pediatric endocrinology

Published: June 25, 2024

A case report of non-lamin A/C dilated cardiomyopathy presenting in a patient with Najjar-Malouf syndrome.

Journal: European heart journal. Case reports

Published: March 04, 2024

Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: February 22, 2023

Early-Onset Diabetes Mellitus in Chromosome 8p11.2 Deletion Syndrome Combined With Becker Muscular Dystrophy - A Case Report.

Journal: Frontiers in endocrinology

Published: April 07, 2022

A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report.

Journal: Endocrine, metabolic & immune disorders drug targets

Published: September 05, 2021

Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.

Journal: Molecular genetics & genomic medicine

Published: January 07, 2021

A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.

Journal: BMC endocrine disorders

Published: December 24, 2020

Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism Latest Advances

Find the Latest Research About Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism

Repair of Ventricular Septal Defect in Children with TAB2 Gene Anomalies and Associated Cardiomyopathy.

Repair of Ventricular Septal Defect in Children with TAB2 Gene Anomalies and Associated Cardiomyopathy.

Progeroid features in a patient with Malouf syndrome due to a rare LMNA variant: a case report and review of the literature.

Progeroid features in a patient with Malouf syndrome due to a rare LMNA variant: a case report and review of the literature.

The Quiet Burden of Iron: A Rare Case of Hereditary Hemochromatosis in Pakistan.

The Quiet Burden of Iron: A Rare Case of Hereditary Hemochromatosis in Pakistan.

Testosterone in Duchenne muscular dystrophy: effects on puberty and growth.

Testosterone in Duchenne muscular dystrophy: effects on puberty and growth.

Possible consequences of the abuse of anabolic steroids on different organs of athletes.

Possible consequences of the abuse of anabolic steroids on different organs of athletes.

Frequency of Delayed Puberty in Boys with Contemporary Management of Duchenne Muscular Dystrophy

Frequency of Delayed Puberty in Boys with Contemporary Management of Duchenne Muscular Dystrophy

A case report of non-lamin A/C dilated cardiomyopathy presenting in a patient with Najjar-Malouf syndrome.

A case report of non-lamin A/C dilated cardiomyopathy presenting in a patient with Najjar-Malouf syndrome.

Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.

Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.

Early-Onset Diabetes Mellitus in Chromosome 8p11.2 Deletion Syndrome Combined With Becker Muscular Dystrophy - A Case Report.

Early-Onset Diabetes Mellitus in Chromosome 8p11.2 Deletion Syndrome Combined With Becker Muscular Dystrophy - A Case Report.

A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report.

A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report.

Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.

Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.

A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.

A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.