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Periostosis

Abnormal deposition of periosteal bone. []
National Institutes of Health

Related topics

Related topics

2 relations
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2Rosenthal-Kloepfer syndrome

Papers overview

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2016
2016
Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis
Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare genetic disease affecting both skin and bones… Expand
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2012
2012
Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.
BACKGROUND Pachydermoperiostosis (PDP) is a rare genetic disorder characterized by 3 major symptoms: pachydermia including cutis… Expand
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2011
2011
Primary hypertrophic osteoarthropathy with digital clubbing and palmoplantar hyperhidrosis caused by 15-PGHD/HPGD loss-of-function mutations.
Digital clubbing is the most prominent feature in primary (PHO) and secondary (pulmonary) hypertrophic osteoarthropathy (HO… Expand
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2010
2010
Treatment of pachydermoperiostosis pachydermia with botulinum toxin type A.
BACKGROUND Pachydermoperiostosis (PDP) is a rare hereditary disorder characterized by digital clubbing, periostosis, and… Expand
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2009
2009
Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy
Mutations in HPGD have recently been reported to cause primary hypertrophic osteoarthropathy (PHO), a rare genetic disease… Expand
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2003
2003
Pachydermoperiostosis associated with juvenile polyps of the stomach and gastric adenocarcinoma
Pachydermoperiostosis (PDP) is a rare syndrome, and the presence of digital clubbing, radiographic periostosis, and coarse facial… Expand
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2001
2001
Primary hypertrophic osteoarthropathy: clinical, radiologic, and scintigraphic characteristics.
BACKGROUND Our aim was to establish clinical and imaging characteristics of primary hypertrophic osteoarthropathy (PHO… Expand
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2001
2001
Indomethacin treatment of infantile cortical periostosis in twins.
Twin girls presented with infantile cortical periostosis (Caffey's disease) at 2 and 3 weeks of age, respectively. This disorder… Expand
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1996
1996
Pachydermoperiostosis (肥大性皮膚骨膜症) の手術例
n engl j med 370;20 nejm.org may 15, 2014 1930 A 32-year-old man of Han Chinese origin presented with a 15-year history of a… Expand
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Review
1991
Review
1991
[Recurrent multifocal periostosis in children. Report of a familial form].
Recurrent multifocal periostosis of childhood is an infrequent disease. All cases reported to date have been sporadic. A familial… Expand
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