Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Endocrinol Nutr ; 56(8): 428-30, 2009 Oct.
Article in Spanish | MEDLINE | ID: mdl-19959154

ABSTRACT

Pendred's syndrome is an autosomal recessive disorder leading to congenital sensorineural hearing loss and a variable degree of goiter due to reduced iodine organification. The cause of this disease is dysfunction of an anion transporter protein located on the apical membrane of thyrocytes, called pendrin, which is also found in the kidney and cochlea. Molecular analysis of the gene is useful to identify other affected family members and provide proper genetic advice and early diagnosis in descendants. We present the cases of two siblings with sensorineural deafness who were diagnosed with Pendred's syndrome as adults because one of them consulted for goiter.


Subject(s)
Goiter/genetics , Hearing Loss, Sensorineural/genetics , Membrane Transport Proteins/genetics , Adult , Biological Transport/genetics , Endolymph/metabolism , Genes, Recessive , Hearing Loss, Sensorineural/congenital , Humans , Incidental Findings , Kidney/metabolism , Male , Membrane Transport Proteins/physiology , Sulfate Transporters , Syndrome , Thyroid Gland/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...