Register and clinical follow-up of patients with Peutz-Jeghers syndrome in Valencia

Autor: F A, Rodríguez Lagos, J V, Sorlí Guerola, I M, Romero Martínez, P, Codoñer Franch

Publikováno v: Revista de gastroenterologia de Mexico (English). 85(2)

Peutz-Jeghers syndrome is a rare autosomal dominant inherited disease caused by a germline mutation of the STK11/LKB1 gene, located on chromosome 19p13.3. It is characterized by mucocutaneous hyperpigmentation, hamartomatous polyposis, and predisposi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6231d512c1811d2ece884cf51146671d
https://pubmed.ncbi.nlm.nih.gov/31257110

Papel del médico de familia en el diagnóstico concomitante de mieloma y amiloidosis primaria en una misma paciente. Caso clínico

Autor: F. Andrea Rodríguez-Lagos, José V. Sorlí, Michelle C. Calviño-Naveira, Nuria Estañ Capell

Publikováno v: Rodríguez Lagos, F. Andrea Sorlí Guerola, José Vicente Calviño Naveira, Michelle C. Estañ Capell, Nuria 2018 Papel del médico de familia en el diagnóstico concomitante de mieloma y amiloidosis primaria en una misma paciente. Caso clínico Revista Medica de Chile 146 11 1351 1355
Revista médica de Chile v.146 n.11 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname

Multiple Myeloma is a myeloproliferative disorder of plasma cells, which may be complicated with secondary amyloidosis. We report a 48 year old woman consulting to primary care for weight loss and malaise. An initial laboratory study revealed a hypog

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6045a91e7ec720450f9cc884f7d3ca4e
http://hdl.handle.net/10550/69175