Results 71 to 80 of about 729 (170)

Cranio-osteoarthropathy in sibs

, 2007
Primary hypertrophic osteoarthropathy is a condition characterized by clubbing, arthropathy and periostosis of long tubular bones. Three variants of primary hypertrophic osteoarthropathy are distinguished: pachydermoperiostosis, which shows as additional
Hennekam, Raoul C. M., Hall, Christine M., Wilson, Louise C., Dabir, Tabib, Sills, A. M., Bennett, Chris   +5 more
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Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy

, 2009
Mutations in HPGD have recently been reported to cause primary hypertrophic osteoarthropathy (PHO), a rare genetic disease characterized by digital clubbing, pachydermia, and periostosis.
Sırmacı, Aslı, Ayten, Guelen Ece, Özdemir, Mustafa, Erdoğan, Yurdanur, Tekin, Mustafa, Yüksel-Konuk, Berrin, Sirmaci, Asli, Yılmaz-Turay, Ülkü, Ayten, Gülen Ece, Yilmaz-Turay, Uelkue, Aslan, İdil   +10 more
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Primary Generalized Hyperostosis in Ancient Peru [PDF]

, 1976
Primary generalized hyperostosis is a rare disease usually diagnosed by radiographic examination. Uehlinger considers this syndrome to be different from the secondary osteoarthropathy of the Marie-Bamberger variety and Paget’s disease.
Gerszten, Enrique, Allison, Marvin J., Pezzia, Alejandro, Sotil, Raul   +3 more
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A novel homozygous splice site mutation in the HPGD gene causes mild primary hypertrophic osteoarthropathy

, 2010
Objectives Homozygous mutations in HPGD gene, encoding 15-hydroxyprostaglandin dehydrogenase, have recently been associated with primary hypertrophic osteoarthropathy (PHO). So far, only 7 HPGD alterations are known. In order to expand this mutational
Brancati F, BOTTILLO, IRENE, Harifi G, Iannicelli M, El Hassani S, Sinibaldi L, Dallapiccola B.   +6 more
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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

Skin changes in chronic lymphatic filariasis.

, 1996
Seventeen men and 31 women with unilateral lower limb lymphoedema attributed to chronic lymphatic filariasis were examined in the filarial out-patient clinic of the Government General Hospital, Madras, India.
Burri H, Kumaraswami V, Vijayasekaran V, Loutan L   +3 more
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Results of surgical treatment of massive localized lymphedema in severely obese patients

Revista do Colégio Brasileiro de Cirurgiões
OBJECTIVE: to evaluate the importance of treatment of deformities caused by massive localized lymphedema (MLL) in the severely obese. METHODS: in a period of seven years, nine patients with morbid obesity and a mean age of 33 years underwent surgical ...
Wilson Cintra Júnior, Miguel Luiz Antonio Modolin, Rodrigo Itocazo Rocha, Thadeu Rangel Fernandes, Ariel Barreto Nogueira, Rolf Gemperli   +5 more
doaj   +1 more source

Osteoartropatía hipertrófica primaria [PDF]

, 2019
Primary hypertrophic osteoarthropathy, pachydermoperiostosis, is a rare genodermatosis. It is characterized by the triad of pachydermia, digital and periostosis changes.
Moreno, María Isabel, Cortés, Carolina, Peñaranda, Elkin Omar   +2 more
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Skin changes in chronic lymphatic filariasis [PDF]

, 2017
Seventeen men and 31 women with unilateral lower limb lymphoedema attributed to chronic lymphatic filariasis were examined in the filarial out-patient clinic of the Government General Hospital, Madras, India.
Loutan, Louis, Burri, Haran, Kumaraswami, V., Vijayasekaran, V.   +3 more
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A Case of Hypertrophic Gastropathy and Early Gastric Cancer Associated with Pachydermoperiostosis [PDF]

, 2000
Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal new bone formation of tubular bones, and hypertrophic skin changes (pachydermia).
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