Albright's Hereditary Osteodystrophy Latest Advances

Find the Latest Research About Albright's Hereditary Osteodystrophy

Last Updated: 09/26/2026

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Found 2001 publications

A Case of Pseudohypoparathyroidism With Unusual Presentation and Novel Genetic Mutation.

A Case of Pseudohypoparathyroidism With Unusual Presentation and Novel Genetic Mutation.

Journal: Cureus
Published: June 18, 2026

Pseudohypoparathyroidism Type 1A in an Omani Family Demonstrating Phenotypic Heterogeneity and Progressive Biochemical Changes.

Pseudohypoparathyroidism Type 1A in an Omani Family Demonstrating Phenotypic Heterogeneity and Progressive Biochemical Changes.

Journal: Cureus
Published: June 15, 2026

Skeletal dysplasias of the parathyroid hormone signaling cascade: radiological manifestations and molecular mechanisms.

Skeletal dysplasias of the parathyroid hormone signaling cascade: radiological manifestations and molecular mechanisms.

Journal: Pediatric radiology
Published: June 15, 2026

LOXL3-related foveal hypoplasia in siblings.

LOXL3-related foveal hypoplasia in siblings.

Journal: Ophthalmic genetics
Published: June 09, 2026

Variability of endocrine findings with age and clinical severity in the long-term follow-up of pseudohypoparathyroidism: evidence of TRH resistance with central hypothyroidism.

Variability of endocrine findings with age and clinical severity in the long-term follow-up of pseudohypoparathyroidism: evidence of TRH resistance with central hypothyroidism.

Journal: Frontiers in endocrinology
Published: May 26, 2026

Adverse health outcomes across the life course in individuals with six rare bone diseases: a 10-year population-based cohort study.

Adverse health outcomes across the life course in individuals with six rare bone diseases: a 10-year population-based cohort study.

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

Pseudohypoparathyroidism with Turner's Syndrome.

Pseudohypoparathyroidism with Turner's Syndrome.

Journal: Indian journal of dermatology
Published: May 11, 2026

Pseudohypoparathyroidism in a Chinese girl: A case report.

Pseudohypoparathyroidism in a Chinese girl: A case report.

Journal: The Journal of international medical research
Published: April 12, 2026

Case Report: Three pathogenic molecular findings in a patient with myotonia congenita, pseudohypoparathyroidism, and a glaucoma-suspect phenotype.

Case Report: Three pathogenic molecular findings in a patient with myotonia congenita, pseudohypoparathyroidism, and a glaucoma-suspect phenotype.

Journal: Frontiers in endocrinology
Published: April 08, 2026

Clinical and genetic characteristics of pseudohypoparathyroidism type 1

Clinical and genetic characteristics of pseudohypoparathyroidism type 1

Journal: Zhonghua yi xue za zhi
Published: April 07, 2026

Normocalcemic pseudohypoparathyroidism type 1B complicated by hypokalemia: A case report.

Normocalcemic pseudohypoparathyroidism type 1B complicated by hypokalemia: A case report.

Journal: SAGE open medical case reports
Published: March 18, 2026

Abnormal position of a GNAS methylation regulatory element causes autosomal dominant pseudohypoparathyroidism type 1B (PHP1B).

Abnormal position of a GNAS methylation regulatory element causes autosomal dominant pseudohypoparathyroidism type 1B (PHP1B).

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: February 16, 2026
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Last Updated: 09/26/2026