(redirected from pachydermoperiostosis)
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PDPProgram Decision Package
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References in periodicals archive ?
Education and imaging: Gastrointestinal: Pachydermoperiostosis associated with Crohn's disease.
Rheumatologic manifestations of pachydermoperiostosis and preliminary experience with bisphosphonates.
After excluding excess GH secretion, the patient was diagnosed as pachydermoperiostosis because of the presence of clubbing, thickening of the skin, hyperhidrosis, hypertrophic osteoarthropathy, arthritis, and acro-osteolysis.
In 1868, Friedrich described pachydermoperiostosis in two young brothers.
The patient was diagnosed with pachydermoperiostosis at age 19.
The most common ocular associations of pachydermoperiostosis are blepharoptosis and tarsitis.
Pachydermoperiostosis (idiopathic clubbing and periostosis) (and genetic and physiologic considerations).
Pachydermoperiostosis (primary hypertrophic osteoarthropathy): report of a case with evidence of endothelial and connective tissue involvement.
Based on clinical features, radiological and histopathological findings, patient was diagnosed as complete form of pachydermoperiostosis.
Pachydermoperiostosis is a rare hereditary disorder which mainly appears as an autosomal dominant pattern with variable penetration.
Pachydermoperiostosis - the complete form of the syndrome.
Type of CVG Associated disease Primary essential CVG None Primary nonessential CVG Neurological: seizures, mental retardation Ocular: cataracts, optic atrophy Secondary * Acromegaly * Amyloidosis * Cylindroma * Connective tissue nevus * Focal mucinosis * Klinefelter syndrome * Leukemia * Myxedema * Melanocyte nevi'hamartomas * Neurofibroma * Nevus lipomatosus * Noonan syndrome * Pachydermoperiostosis * Tuberous sclerosis * Turner syndrome CVG Cutis verticis gyrata