Results 81 to 90 of about 944 (190)

Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome? [PDF]

, 2011
Ectopic liver is a very uncommon developmental anomaly that predisposes to the development of hepatocellular carcinoma. We describe the second documented case of a hepatocellular carcinoma developing in the primary liver of a patient with a rare and ...
Dettmer, Matthias, Itin, Peter, Miny, Peter, Gandhi, Manoj, Cathomas, Gieri, Willi, Niels   +5 more
core   +5 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, Dipti Sarma, Uma Saikia   +2 more
doaj   +1 more source

Novel SLCO2A1 mutations cause gender-differentiated pachydermoperiostosis [PDF]

, 2018
Primary hypertrophic osteoarthropathy (PHO) is a rare familial disorder with reduced penetrance for females. The genetic mutations associated with PHO have been identified in HPGD and SLCO2A1, which involved in prostaglandin E2 metabolism.
Dan Wu, Guoqiang Bao, Jianguo Lu, Lifeng Wang, Lijuan Yuan, Sijia Zhang, Xihui Chen, Yuanming Wu, Ziyu Liu   +8 more
core   +1 more source

Revista de Științe ale Sănătății din Moldova = Moldovan Journal of Health Sciences. 2023, Vol. 10(2) [PDF]

, 2023
Revista de Științe ale Sănătății din Moldova (Moldovan Journal of Health Sciences) a fost lansată în octombrie 2014. Aceasta este editată în limbile română și engleză, conform standardelor și ghidurilor internaționale actuale în domeniul științelor ...

core  

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, Débora Cadore de Farias, Marcus Maia, Helena Müller   +3 more
doaj   +1 more source

Familial primary osteoarthropathy: A case report with unusual dental findings

Journal of Indian Academy of Oral Medicine and Radiology, 2015
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.
Vela D Desai, Sunil MV Kumar, Sahil Maghu   +2 more
doaj   +1 more source

Pachydermoperiostosis [PDF]

BMJ, 1962
K. Shawarby, M. S. Ibrahim
openaire   +2 more sources

Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis

JPRAS Open, 2019
Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal ...
Nutthawut Akaranuchat, Papassorn Limsuvan   +1 more
doaj   +1 more source

Pseudoacromegaly: A Differential Diagnostic Problem for Acromegaly With a Genetic Solution. [PDF]

, 2017
Acromegaly is usually not a difficult condition to diagnose once the possibility of this disease has been raised. However, a few conditions present with some aspects of acromegaly or gigantism but without growth hormone (GH) excess.
Dahlqvist, P, Dang, MN, Glad, CAM, Johannsson, G, Korbonits, M, Marques, P, Spencer, R   +6 more
core   +1 more source

Arthroscopic synovectomy and radiosynoviorthesis: a treatment option for recurrent arthritis symptoms in patients with pachydermoperiostosis

Reumatismo, 2013
Pachydermoperiostosis as the primary form of hypertrophic osteoarthropathy is a rare hereditary disorder with a number of characteristic findings, e.g. periosteal hypertrophy, digital clubbing and pachydermia.
S. Warwas, C. Specker, M. Jäger, S. Landgraeber   +3 more
doaj   +1 more source