Cutaneous telangiectasias, sparse hair, and type I membranoproliferative glomerulonephritis

Autor:	Indra R. Gupta, Paul S. Thorner, J W Balfe, J. Siegel-Bartelt, C. H. Tsai
Rok vydání:	1999
Předmět:	congenital hereditary and neonatal diseases and abnormalities Ectodermal dysplasia medicine.medical_specialty Glomerulonephritis Membranoproliferative Kidney Function Tests Heart Septal Defects Atrial Membranoproliferative glomerulonephritis Medicine Humans cardiovascular diseases Telangiectasis Sparse hair Telangiectasia Child Eyelashes business.industry Alopecia medicine.disease Dermatology Surgery Nephrology Pediatrics Perinatology and Child Health Mesangial proliferative glomerulonephritis Female medicine.symptom Congenital disease Eyebrows business
Zdroj:	Pediatric nephrology (Berlin, Germany). 13(2)
ISSN:	0931-041X
Popis:	We report the unusual association of normocomplementemic type I membranoproliferative glomerulonephritis in a 10-year-old girl with sparse red hair, absent eyebrows and eyelashes, cutaneous telangiectasias, and an atrial septal defect.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c95f73eeb3756b5065714939e613b02 https://pubmed.ncbi.nlm.nih.gov/10228999 Zobrazit plný text záznamu Plný text ve formátu PDF