Hypophosphatasia (HPP) Latest Advances

Find the Latest Research About Hypophosphatasia (HPP)

Last Updated: 09/26/2026

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Found 1655 publications

Possible adult-onset hypophosphatasia variant presenting as young-onset parkinsonism with limited levodopa responsiveness.

Possible adult-onset hypophosphatasia variant presenting as young-onset parkinsonism with limited levodopa responsiveness.

Journal: BMJ case reports
Published: August 17, 2026

Hypophosphatasia: Results of a Country-Wide Selective Screening Program Using NGS Technology as a First-Tier Test.

Hypophosphatasia: Results of a Country-Wide Selective Screening Program Using NGS Technology as a First-Tier Test.

Journal: International journal of molecular sciences
Published: July 06, 2026

Odonto-hypophosphatasia with Tooth Agenesis: a Case Report.

Odonto-hypophosphatasia with Tooth Agenesis: a Case Report.

Journal: The Chinese journal of dental research
Published: June 30, 2026

Osteoglycin and Sclerostin Imbalance in Hypophosphatasia: Bone-Derived Markers of Mineralization and Systemic Involvement.

Osteoglycin and Sclerostin Imbalance in Hypophosphatasia: Bone-Derived Markers of Mineralization and Systemic Involvement.

Journal: International journal of molecular sciences
Published: June 26, 2026

Correction: Transition Care for Young People with Rare Bone and Mineral Conditions: A Scoping Review.

Correction: Transition Care for Young People with Rare Bone and Mineral Conditions: A Scoping Review.

Journal: Advances in therapy
Published: June 18, 2026

Attitudes of people with lived experience of hypophosphatasia (HPP) toward in-utero enzyme replacement therapy (IU-ERT) for life-threatening HPP.

Attitudes of people with lived experience of hypophosphatasia (HPP) toward in-utero enzyme replacement therapy (IU-ERT) for life-threatening HPP.

Journal: Molecular genetics and metabolism
Published: June 17, 2026

Evolving Therapeutic Paradigms in Pediatric Hypophosphatasia: From Survival-Driven Care to Integrated Precision Management.

Evolving Therapeutic Paradigms in Pediatric Hypophosphatasia: From Survival-Driven Care to Integrated Precision Management.

Journal: International journal of molecular sciences
Published: May 31, 2026

Prevalence of clinical manifestations among patients with hypophosphatasia in Central and Eastern European countries.

Prevalence of clinical manifestations among patients with hypophosphatasia in Central and Eastern European countries.

Journal: Frontiers in endocrinology
Published: May 27, 2026

The Journal of Bone and Mineral Research (JBMR) 40th anniversary celebration: the fourth decade (Part 2).

The Journal of Bone and Mineral Research (JBMR) 40th anniversary celebration: the fourth decade (Part 2).

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: May 04, 2026

Case Report: Cortical bone loss, impaired mineralization, and reduced adiposity contributing to chronic bone pain in SFRP4-related skeletal disease with an ALPL variant.

Case Report: Cortical bone loss, impaired mineralization, and reduced adiposity contributing to chronic bone pain in SFRP4-related skeletal disease with an ALPL variant.

Journal: Frontiers in endocrinology
Published: May 01, 2026

Osteogenesis Imperfecta Type 4 With COL1A2 c.1135G>A (p.Gly379Arg) Variant: Unmodified by Concurrent ALPL c.1559delT (p.Leu520ArgfsTer86) Carrier Status: A Case Report.

Osteogenesis Imperfecta Type 4 With COL1A2 c.1135G>A (p.Gly379Arg) Variant: Unmodified by Concurrent ALPL c.1559delT (p.Leu520ArgfsTer86) Carrier Status: A Case Report.

Journal: Cureus
Published: April 30, 2026

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Journal: Human genome variation
Published: April 21, 2026
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Last Updated: 09/26/2026