Pachydermoperiostosis (PDP) is a rare osteo-arthro-dermopathic syndrome, the diagnosis of which can be made on the basis of the classic clinical and radiological presentations. The primary form of the disease, also called as Touraine-Solente-Gole Syndrome, contributes to approximately 3-5% of the cases of hypertrophic osteoarthropathy (HOA). The authors present here a rare case of familial primary osteoarthropathy with significant dental findings which, to the best of our knowledge, is seldom reported in English literature
Primary hypertrophic osteoarthropathy is a rare hereditary disease without evidence of underlying di...
We report a family with pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy) spanning fo...
Familial osteodysplasia is a disorder of osteogenesis with an autosomal recessive pattern of inherit...
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy is a rare syndrome with diverse...
Pachydermoperiostosis or Touraine-Solente-Gole syndrome is a rare genetic disorder that follows auto...
PubMed ID: 2001143049Pachydermoperiostosis (PDP) is an unusual syndrome manifested clinically by fin...
Primary hypertrophic osteoarthropathy (HOA), or pachydermoperiostosis, is a rare benign disorder of ...
Neste artigo apresentamos dois irmãos acometidos pela osteoartropatia hipertrófica primária (paquide...
Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic or...
Pachydermoperiostosis is a rare hereditary disorder, which affects both bones and skin. It is charac...
Five patients with pachydermoperiostosis are described. Three ofthem showed the incomplete form, and...
A father and daughter both had multiple pathological fractures and nodal osteoarthropathy. The fathe...
Touraine-Solente-Gole syndrome, also known as pachydermoperiostosis, is transmitted as an autosomal ...
The paper gives the data available in the literature on the relatively rare disease hypertrophic ost...
Abstract Hajdu-Cheney syndrome is a rare, probably autosomal dominant connective tissue disorder wit...
Primary hypertrophic osteoarthropathy is a rare hereditary disease without evidence of underlying di...
We report a family with pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy) spanning fo...
Familial osteodysplasia is a disorder of osteogenesis with an autosomal recessive pattern of inherit...
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy is a rare syndrome with diverse...
Pachydermoperiostosis or Touraine-Solente-Gole syndrome is a rare genetic disorder that follows auto...
PubMed ID: 2001143049Pachydermoperiostosis (PDP) is an unusual syndrome manifested clinically by fin...
Primary hypertrophic osteoarthropathy (HOA), or pachydermoperiostosis, is a rare benign disorder of ...
Neste artigo apresentamos dois irmãos acometidos pela osteoartropatia hipertrófica primária (paquide...
Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic or...
Pachydermoperiostosis is a rare hereditary disorder, which affects both bones and skin. It is charac...
Five patients with pachydermoperiostosis are described. Three ofthem showed the incomplete form, and...
A father and daughter both had multiple pathological fractures and nodal osteoarthropathy. The fathe...
Touraine-Solente-Gole syndrome, also known as pachydermoperiostosis, is transmitted as an autosomal ...
The paper gives the data available in the literature on the relatively rare disease hypertrophic ost...
Abstract Hajdu-Cheney syndrome is a rare, probably autosomal dominant connective tissue disorder wit...
Primary hypertrophic osteoarthropathy is a rare hereditary disease without evidence of underlying di...
We report a family with pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy) spanning fo...
Familial osteodysplasia is a disorder of osteogenesis with an autosomal recessive pattern of inherit...