Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy, is a
rare genetic disorder characterized by pachyderma and periostosis. Acromegaly is a …

Case 3: A 20 yr old male, born to a non-consanguineous couple of north Indian ethnicity,
presented on December 22, 2014, with bilateral swelling of ankle joints. On examination, he …

Abstract Introduction: Pachydermoperiostosis (PDP), or primary hypertrophic
osteoarthropathy, is a rare autosomal dominant disease with primary clinical features of …

Here, we highlight the case of a 31-yr-old man who had clinical features of primary
hypertrophic osteoarthropathy (PHOAR) and harbored a homozygous variant (c. 38C> A, p …

Background Hypertrophic osteoarthropathy (HOA) is a rare and intricate hereditary disease.
The appearance and functional deformity of the forehead caused by thickened folds are the …

Touraine-Solente-Gole syndrome is a rare, autosomal dominant multisystem disorder
arising from dysregulated prostaglandin synthesis due to underlying genetic defects. Early …

On the flip side, the lack of illustrations such as figures and line diagrams seems like some
sort of shortcoming. The editor should have provided 'key points at the end of each chapter' …

Pachydermoperiostosis, also known as Touraine-Solente-Golé syndrome, is an uncommon
hereditary condition. This condition includes skin thickening (pachydermia), abnormalities of …

A 24-year-old Thai male presented to our outpatient department with a chief complaint of
progressive thickening and furrowing of facial skin and scalp for 7 years. He also …

Pachydermoperiostosis, a rare condition, is characterized by pachydermia, finger clubbing,
and periostosis. We present an unusual treatment for frontal rhytids, for which we used a …