Infantile nephrotic syndrome with prominent facial dysmorphism: A possible case of Galloway-Mowat syndrome

Autor: Ahmed,Ayaz, Khalid,Adeel, Qaiser,Habib, Sajjad,Reema, Qader,Saima, Hashmi,Seema, Lanewala,Ali, Kazi,Javed Iqbal, Mubarak,Muhammed

Publikováno v: Portuguese Journal of Nephrology & Hypertension, Volume: 28, Issue: 2, Pages: 154-159, Published: JUN 2014
Portuguese Journal of Nephrology & Hypertension v.28 n.2 2014
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Galloway-Mowat syndrome is a rare hereditary disorder originally described as a triad of early-onset nephrotic syndrome, microcephaly, and hiatus hernia. Subsequent reports have expanded the clinical and pathological spectrum of the disorder. We desc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6c777b026c091d4931c0dbbcc4ae7162
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692014000200009&lng=en&tlng=en

URINARY INCONTINENCE-PATIENT'S PHYSICAL, MENTAL AND ORAL HEALTH ANALYSIS.

Autor: ALI, SYED IMTIAZ, HANIF, HAMMAD, TANWIR, FARZEEN, PERVAIZ, SHAHEER, SAJJAD, REEMA, PERVAIZ, HASEEB, RANGHA, ALI NAWAZ, HASHMI, SHAHKAMAL

Publikováno v: Pakistan Oral & Dental Journal; 9/30/2014, Vol. 34 Issue 3, p515-519, 5p