Familial Hypopituitarism Latest Advances

Find the Latest Research About Familial Hypopituitarism

Last Updated: 09/26/2026

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Found 920 publications

Rare Endocrine Disorders in Children of Consanguineous Parents: A Case Series.

Rare Endocrine Disorders in Children of Consanguineous Parents: A Case Series.

Journal: Cureus
Published: July 15, 2026

A Novel LHX3 Variant Associated With Combined Pituitary Hormone Deficiency in an Indian Kindred.

A Novel LHX3 Variant Associated With Combined Pituitary Hormone Deficiency in an Indian Kindred.

Journal: Cureus
Published: June 29, 2026

Long-term clinical trajectory of microvillus inclusion disease associated with STXBP2-related familial hemophagocytic lymphohistiocytosis type 5: A case report.

Long-term clinical trajectory of microvillus inclusion disease associated with STXBP2-related familial hemophagocytic lymphohistiocytosis type 5: A case report.

Journal: JPEN. Journal of parenteral and enteral nutrition
Published: June 20, 2026

Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.

Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.

Journal: Clinical endocrinology
Published: June 10, 2026

Trauma Unmasking Pituitary Apoplexy: Coexisting Epidural Hematoma and Sellar Mass - A Case Report with Selected Cases from the Literature.

Trauma Unmasking Pituitary Apoplexy: Coexisting Epidural Hematoma and Sellar Mass - A Case Report with Selected Cases from the Literature.

Journal: International medical case reports journal
Published: April 20, 2026

CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.

CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.

Journal: European journal of endocrinology
Published: March 23, 2026

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

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 11, 2026

Patient-reported outcomes in a Pituitary Tumor Center of Excellence (PTCOE)-aligned pituitary clinic compared with general endocrinology care.

Patient-reported outcomes in a Pituitary Tumor Center of Excellence (PTCOE)-aligned pituitary clinic compared with general endocrinology care.

Journal: Pituitary
Published: March 02, 2026

Unraveling the Genetic Heterogeneity of Isolated Growth Hormone Deficiency: Insights from the GENHYPOPIT Cohort.

Unraveling the Genetic Heterogeneity of Isolated Growth Hormone Deficiency: Insights from the GENHYPOPIT Cohort.

Journal: Hormone research in paediatrics
Published: February 09, 2026

X-linked spondyloepiphyseal dysplasia tarda misdiagnosed as growth hormone deficiency: identification of a novel intronic TRAPPC2 variant by whole-genome sequencing.

X-linked spondyloepiphyseal dysplasia tarda misdiagnosed as growth hormone deficiency: identification of a novel intronic TRAPPC2 variant by whole-genome sequencing.

Journal: BMC pediatrics
Published: February 09, 2026

Hypopituitarism in patients with prolactinomas: a narrative review.

Hypopituitarism in patients with prolactinomas: a narrative review.

Journal: Best practice & research. Clinical endocrinology & metabolism
Published: February 04, 2026

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.

Journal: Cureus
Published: February 01, 2026
Showing 1-12 of 920

Last Updated: 09/26/2026