Pachydermoperiostosis Latest Advances

When Myelofibrosis is Skin-Deep: A Clinical Clue to a Rare Diagnosis

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: March 27, 2026

Primary hypertrophic osteoarthropathy presenting with ptosis and floppy eyelids: a review of ophthalmic manifestations, histopathology, and pathophysiology.

Journal: Orbit (Amsterdam, Netherlands)

Published: February 20, 2026

P19 A rare case of PHOAR2-enteropathy syndrome (PHOAR2E; previously known as pachydermoperiostosis) with a causal variant in the SLCO2A1 gene.

Journal: The British journal of dermatology

Published: December 18, 2025

Pachydermoperiostosis Presenting With Gynecomastia and Low Insulin-Like Growth Factor-1 Levels: A Diagnostic Challenge.

Journal: Cureus

Published: December 17, 2025

A Rare Case of Primary Hypertrophic Osteoarthropathy Secondary to SLCO2A1 Gene Mutation.

Journal: The Journal of the Association of Physicians of India

Published: November 26, 2025

From Juvenile Idiopathic Arthritis to Pachydermoperiostosis: A Journey to an Unexpected Rare Diagnosis.

Journal: Journal of clinical medicine

Published: November 23, 2025

A rare clinical image of pachydermoperiostosis (Touraine-Solente-Gole syndrome).

Journal: The Pan African medical journal

Published: October 07, 2025

Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review.

Journal: Cureus

Published: September 19, 2025

Elevated calcitonin gene-related peptide expression through prostaglandin E2-EP4 receptor pathway in promoting proliferative periosteum formation in primary hypertrophic osteoarthropathy.

Journal: Journal of orthopaedic translation

Published: July 18, 2025

A Loss-of-Function Variant Causing Primary Autosomal Recessive Hypertrophic Osteoarthropathy.

Journal: Cureus

Published: July 17, 2025

Bone Density, Microarchitecture, and Geometry Assessment in Patients with Pachydermoperiostosis Using Second-Generation High-Resolution Peripheral Quantitative Computed Tomography: A Case-Control Study.

Journal: Calcified tissue international

Published: May 29, 2025

Primary Hypertrophic Osteoarthropathy-A Rare Cause of Joint Pain.

Journal: The Journal of the Association of Physicians of India

Published: April 09, 2025

Pachydermoperiostosis Latest Advances

Find the Latest Research About Pachydermoperiostosis

When Myelofibrosis is Skin-Deep: A Clinical Clue to a Rare Diagnosis

When Myelofibrosis is Skin-Deep: A Clinical Clue to a Rare Diagnosis

Primary hypertrophic osteoarthropathy presenting with ptosis and floppy eyelids: a review of ophthalmic manifestations, histopathology, and pathophysiology.

Primary hypertrophic osteoarthropathy presenting with ptosis and floppy eyelids: a review of ophthalmic manifestations, histopathology, and pathophysiology.

P19 A rare case of PHOAR2-enteropathy syndrome (PHOAR2E; previously known as pachydermoperiostosis) with a causal variant in the SLCO2A1 gene.

P19 A rare case of PHOAR2-enteropathy syndrome (PHOAR2E; previously known as pachydermoperiostosis) with a causal variant in the SLCO2A1 gene.

Pachydermoperiostosis Presenting With Gynecomastia and Low Insulin-Like Growth Factor-1 Levels: A Diagnostic Challenge.

Pachydermoperiostosis Presenting With Gynecomastia and Low Insulin-Like Growth Factor-1 Levels: A Diagnostic Challenge.

A Rare Case of Primary Hypertrophic Osteoarthropathy Secondary to SLCO2A1 Gene Mutation.

A Rare Case of Primary Hypertrophic Osteoarthropathy Secondary to SLCO2A1 Gene Mutation.

From Juvenile Idiopathic Arthritis to Pachydermoperiostosis: A Journey to an Unexpected Rare Diagnosis.

From Juvenile Idiopathic Arthritis to Pachydermoperiostosis: A Journey to an Unexpected Rare Diagnosis.

A rare clinical image of pachydermoperiostosis (Touraine-Solente-Gole syndrome).

A rare clinical image of pachydermoperiostosis (Touraine-Solente-Gole syndrome).

Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review.

Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review.

Elevated calcitonin gene-related peptide expression through prostaglandin E2-EP4 receptor pathway in promoting proliferative periosteum formation in primary hypertrophic osteoarthropathy.

Elevated calcitonin gene-related peptide expression through prostaglandin E2-EP4 receptor pathway in promoting proliferative periosteum formation in primary hypertrophic osteoarthropathy.

A Loss-of-Function Variant Causing Primary Autosomal Recessive Hypertrophic Osteoarthropathy.

A Loss-of-Function Variant Causing Primary Autosomal Recessive Hypertrophic Osteoarthropathy.

Bone Density, Microarchitecture, and Geometry Assessment in Patients with Pachydermoperiostosis Using Second-Generation High-Resolution Peripheral Quantitative Computed Tomography: A Case-Control Study.

Bone Density, Microarchitecture, and Geometry Assessment in Patients with Pachydermoperiostosis Using Second-Generation High-Resolution Peripheral Quantitative Computed Tomography: A Case-Control Study.

Primary Hypertrophic Osteoarthropathy-A Rare Cause of Joint Pain.

Primary Hypertrophic Osteoarthropathy-A Rare Cause of Joint Pain.