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Werner's syndrome in a Nigerian: case report

Central African Journal of Medicine 37(2): 63-67

Werner's syndrome in a Nigerian: case report

Accession: 034232031

PMID: 2060015

Related references

Gaetani, S.A.; Ferraris, A.M.; D'Agosta, A., 1988: Case report 485: Werner syndrome. Skeletal Radiology 17(4): 298-301

Ye, Y.; Li, H-qi., 2011: Report of a case with Werner's syndrome. Zhonghua Er Ke Za Zhi 47(3): 228-229

Pomeranz, M.M., 1948: Werner's syndrome; a case report. Radiology 51(4): 521-524

Mateos Romero, L.; Porta Aznares, M.N., 1992: Werner's syndrome. Report of a new case. Werner syndrome or adult progeria is a very rare disease transmitted in a recessive autosomic way. It is characterized by a pathologic and premature aging in all organs and systems, which begins generally between 1st and 3rd decades of life. We di...

Müller, J.; Kunková, A.; Kepertová, A., 1969: Werner's syndrome. (case report). Wiener Zeitschrift für Innere Medizin und Ihre Grenzgebiete 50(3): 112-116

Tamori, Y.; Takahashi, T.; Nakajima, S.; Nishimoto, Y.; Ohno, K.; Takemoto, M.; Yokote, K.; Kita, T.; Tsutsumi, M., 2011: Case report: A case of Werner syndrome with compound heterozygous mutations of WRN gene. Nihon Naika Gakkai Zasshi. Journal of the Japanese Society of Internal Medicine 100(6): 1642-1644

Courel, M., 1970: Rothmund-Werner syndrome (report of a case). Revista Clinica Espanola 117(5): 517-520

Kawauchi, M.; Gibo, H.; Kobayashi, S.; Sugita, K., 1988: Werner's syndrome associated with meningioma: case report. We present two cases of Werner's syndrome associated with intracranial meningioma. Characteristic clinical features of Werner's syndrome include short stature with slender extremities, premature senility, juvenile cataract, skin changes,...

Reynolds, C.; O'Duffy, J.D.; Sams, W.M., 1972: Werner's syndrome. Case report of A variant. Minnesota Medicine 55(10): 917-921

Lok, C.; Ruto, F.; Labeille, B.; Pietri, J.; Denoeux, J.P., 1991: Leg ulcers in Werner's syndrome. Report of one case. Werner's syndrome (adult progeria) is a rare autosomal recessive condition characterized mainly by a characteristic habitus (short stature, light body weight) scleroderma like changes of the limbs and premature aging. Chronic leg ulcers appea...