Familial Hypopituitarism Latest Advances

Genetic analysis of a Chinese pedigree affected with Isolated growth hormone deficiency due to variant of CHRHR gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 11, 2026

Delayed Diagnosis of Sheehan's Syndrome Following Postpartum Hemorrhage and Emergency Hysterectomy: A Case Report.

Journal: Cureus

Published: February 01, 2026

Clinical Challenges in Transition to Adult Care for Young People With Endocrinopathies.

Journal: Clinical endocrinology

Published: December 17, 2025

New insights into Oliver-McFarlane syndrome: adrenocortical hypofunction and variable expressivity in a Chinese sibling pair.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 12, 2025

HRQoL in Adolescents with Idiopathic Isolated GHD: rhGH (Dis)continuation in Mid-Puberty.

Journal: Endocrine connections

Published: December 03, 2025

Identification of a Novel Nonsense Mutation in the IGSF1 Gene Reveals Sex-Specific Phenotypic Variability Within a Single Family.

Journal: Children (Basel, Switzerland)

Published: October 24, 2025

Growth hormone deficiency in three siblings homozygous for a rare GH1 haplotype.

Journal: Frontiers in endocrinology

Published: September 14, 2025

Pituitary hormone deficiencies in prolactinomas: prevalence, predictors, and functional recovery.

Journal: Frontiers in endocrinology

Published: September 14, 2025

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency.

Journal: European journal of pediatrics

Published: September 10, 2025

Stiff-person syndrome mimic secondary to hypopituitarism: a case report and literature review.

Journal: Frontiers in endocrinology

Published: July 12, 2025

Biallelic pathogenic variants in POMC can cause combined pituitary hormonal deficiency associated with severe obesity.

Journal: European journal of endocrinology

Published: April 05, 2025

Quality of life and treatment burden of children receiving daily growth hormone treatment in Greece.

Journal: Endocrine

Published: March 21, 2025

Familial Hypopituitarism Latest Advances

Find the Latest Research About Familial Hypopituitarism

Genetic analysis of a Chinese pedigree affected with Isolated growth hormone deficiency due to variant of CHRHR gene

Genetic analysis of a Chinese pedigree affected with Isolated growth hormone deficiency due to variant of CHRHR gene

Delayed Diagnosis of Sheehan's Syndrome Following Postpartum Hemorrhage and Emergency Hysterectomy: A Case Report.

Delayed Diagnosis of Sheehan's Syndrome Following Postpartum Hemorrhage and Emergency Hysterectomy: A Case Report.

Clinical Challenges in Transition to Adult Care for Young People With Endocrinopathies.

Clinical Challenges in Transition to Adult Care for Young People With Endocrinopathies.

New insights into Oliver-McFarlane syndrome: adrenocortical hypofunction and variable expressivity in a Chinese sibling pair.

New insights into Oliver-McFarlane syndrome: adrenocortical hypofunction and variable expressivity in a Chinese sibling pair.

HRQoL in Adolescents with Idiopathic Isolated GHD: rhGH (Dis)continuation in Mid-Puberty.

HRQoL in Adolescents with Idiopathic Isolated GHD: rhGH (Dis)continuation in Mid-Puberty.

Identification of a Novel Nonsense Mutation in the IGSF1 Gene Reveals Sex-Specific Phenotypic Variability Within a Single Family.

Identification of a Novel Nonsense Mutation in the IGSF1 Gene Reveals Sex-Specific Phenotypic Variability Within a Single Family.

Growth hormone deficiency in three siblings homozygous for a rare GH1 haplotype.

Growth hormone deficiency in three siblings homozygous for a rare GH1 haplotype.

Pituitary hormone deficiencies in prolactinomas: prevalence, predictors, and functional recovery.

Pituitary hormone deficiencies in prolactinomas: prevalence, predictors, and functional recovery.

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency.

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency.

Stiff-person syndrome mimic secondary to hypopituitarism: a case report and literature review.

Stiff-person syndrome mimic secondary to hypopituitarism: a case report and literature review.

Biallelic pathogenic variants in POMC can cause combined pituitary hormonal deficiency associated with severe obesity.

Biallelic pathogenic variants in POMC can cause combined pituitary hormonal deficiency associated with severe obesity.

Quality of life and treatment burden of children receiving daily growth hormone treatment in Greece.

Quality of life and treatment burden of children receiving daily growth hormone treatment in Greece.