Results 51 to 60 of about 2,068 (238)
Rhytidectomy for pachydermoperiostosis
Neha Taneja+2 more
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Bilateral Ptosis Due to a Rare Cause-Pachydermoperiostosis [PDF]
Pachydermoperiostosis is a rare hereditary disorder that is characterised by pachydermia (thickening of the facial skin and/ or scalp), and periostosis (swelling of the periarticular tissue and a subperiosteal new bone formation).
Mahesh M, K V K S N Murthy
doaj +1 more source
The many symptoms of pachydermoperiostosis
A 26-year-old black man with a 3-year history of persistent joint pain and swelling of the wrists and ankles and enlargement of his hands and feet, also reported ‘deformity’ of his fingernails (clubbing) since childhood. His father had similar symptoms, but no siblings were affected.
Bilal Abdool-Gafoor
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Nosology of genetic skeletal disorders: 2023 revision
Abstract The “Nosology of genetic skeletal disorders” has undergone its 11th revision and now contains 771 entries associated with 552 genes reflecting advances in molecular delineation of new disorders thanks to advances in DNA sequencing technology.
Sheila Unger+20 more
wiley +1 more source
Pseudoacromegaly in pachydermoperiostosis [PDF]
A 19-year-old male patient presented with a year-long history of progressive painful enlargement of his hands and feet associated with excessive sweating and greasiness of the face, palms and soles. He also noticed pain over his wrists and ankles without any symptoms suggestive of raised intracranial tension and no recent increase in height.
Rana Bhattacharjee+3 more
openaire +2 more sources
Abstract Background Eczema is the most common form of dermatitis and also the starting point of atopic march. Although many eczema‐associated allergic and immunologic disorders have been studied, there remains a gap in the systematic quantitative knowledge regarding the relationships between all childhood disorders and eczema.
Huiwen Zheng+6 more
wiley +1 more source
Coexistence of Touraine-Solente-Gole syndrome and type 1 neurofibromatosis: A case report
Pachydermoperiostosis is a rare syndrome that affects the skin and skeletal system. Mutations in the gene encoding hydroxyprostaglandin dehydrogenase (HPGD) are thought to play a role in disease etiopathogenesis.
Selma Korkmaz+5 more
doaj +1 more source
Schizophrenia is associated to somatic diseases. We describe an association with hypertrophic osteoarthropathy (HPO). It is a rare clinical entity but it could be a paraneoplastic syndrome hiding a life‐threatening condition. Abstract Schizophrenia is associated to somatic disorders especially cardio‐vascular and auto‐immune.
Emna Baklouti+3 more
wiley +1 more source
Cutis verticis gyrata in a patient with multiple basal cell carcinomas; case presentation and review of the literature [PDF]
Cutis verticis gyrata is a rare disease characterized by convoluted folds and deep furrows of the scalp, resembling the gyri and sulci of the cerebral cortex.
Benea, Vasile+6 more
core +4 more sources
Patrick Rock, Yuranga Weerakkody
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