Results 101 to 110 of about 2,048 (238)
Transgrediens pachydermodactyly: report of a case [PDF]
, 2009 Pachydermodactyly is a rare form of digital fibromatosis involving the proximal portions of the fingers that usually affects young males. We present a 25-year-old male patient with a twoyear history of asymptomatic nodules in the fingers.
Coeli, Flávia Regina +4 more
core +3 more sources
Pachydermoperiostosis (Touraine–Solente–Gole syndrome) imitating Acromegaly
International Journal of Clinical Images and Medical Reviews, 2022 Pachydermoperiostosis (PDP), also known as Touraine-Solente-Golé syndrome/Rosenfeld-Kloepfer syndrome/primary or idiopathic Hypertrophic osteoarthropathy, is an autosomal-dominant/autosomal recessive inherited disorder with variable expression.
R. Gomes
semanticscholar +1 more source
Chloride channels in astrocytes: structure, roles in brain homeostasis and implications in disease [PDF]
, 2020 Astrocytes are the most abundant cell type in the CNS (central nervous system). They exert multiple functions during development and in the adult CNS that are essential for brain homeostasis.
Elorza-Vidal, Xabier +2 more
core +1 more source
Pachydermoperiostosis with Chronic Diarrhoea: A Case Report
Bangladesh Medical Journal, 2022 Pachydermoperiostosis (PDP) is a rare autosomal disorder characterized by periostosis, clubbing, thickening of the skin (pachyderma) of the face and scalp, seborrhea and hyperhydrosis.
M. A. H. Khan +3 more
semanticscholar +1 more source
Crohn’s disease associated with pachydermoperiostosis [PDF]
, 1999 Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal change, pachydermia and autonomic nervous system symptoms such as facial flushing and hy perhidrosis.
김원호
core
A Case Report on Pachydermoperiostosis with Severe Anemia
International journal of pharmaceutical sciences review and research, 2022 Pachydermoperiostosis (PDP), commonly known as primary hypertrophic osteoarthropathy, is a hereditary disorder. The primary characteristics are digital clubbing, pachydermia of the face, hyperhidrosis, cutis vertices gyrate, and polyarthritis.
Purna Chandu +4 more
semanticscholar +1 more source
A Case Report of Pachydermoperiostosis by Multidisciplinary Diagnosis and Treatment
罕见病研究A 20-year-old male patient presented to the Department of Dermatology of Peking Union Medical College Hospital with complaints of an 8-year history of facial scarring, swelling of the lower limbs, and a 4-year history of scalp thickening.
ZHANG Jie +16 more
doaj +1 more source
Pachydermoperiostosis: A clinicopathological description
Journal of Current Ophthalmology, 2019 PURPOSE: To report a case of pachydermoperiostosis (PDP) and a review of the literature. METHODS: A 32-year-old man was referred to our clinic with bilateral eyelid swelling and blepharoptosis. On examination, marked blepharoptosis was noted, and his eyelids were found to be floppy.
Seyed Mohsen Rafizadeh +8 more
openaire +2 more sources
Enlarged hands and feet - Not always acromegaly
Indian Journal of Endocrinology and Metabolism, 2012 Pachydermoperiostosis maybe mistaken for acromegaly as it can present with progressive enlargement of hands and feet. We describe a 32 year old male with enlargement of hands and feet and extensive keloid formation.
Vikrant Ghatnatti +2 more
doaj +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2007 Paquidermoperiostose é genodermatose autossômica dominante rara, que afeta pele e ossos, porém sua prevalência e incidência permanecem desconhecidas. Ocorre predominantemente em homens, que também mostram fenótipo mais grave da doença.
Roberta Buense Bedrikow +3 more
doaj +1 more source