Linked Life Data

19347818

Source:http://linkedlifedata.com/resource/pubmed/id/19347818

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2009-4-6
pubmed:abstractText
The authors describe a case of an adult woman with congenital adrenal hyperplasia caused by 11beta-hydroxylase deficiency. The patient presented not only typical features of this disease such as virilization and hypokaliemic hypertension but also rare pathologies, such as ectopic adrenal tissues, salt loss during infancy, and functional adrenomedullary hyperactivity. In spite of the severe disease and delays in its diagnosis and adequate treatment, significant improvement in appearance and normalization of blood pressure as well as the birth of a healthy child were achieved. The paper also discusses current opinions concerning the pathogenesis and treatment in CAH with 11beta-hydroxylase deficiency as well as difficulties in diagnostic and therapeutic management.
pubmed:language
pol
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0423-104X
pubmed:author
pubmed:issnType
Print
pubmed:volume
59
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
521-9
pubmed:meshHeading
pubmed:articleTitle
[Congenital adrenal hyperplasia caused by 11beta-hydroxylase deficiency. A case report].
pubmed:affiliation
Wrodzony przerost nadnerczy wywo?any niedoborem11b-hydroksylazy. Opis przypadku. szymczak@kom-net.pl
pubmed:publicationType
Journal Article, English Abstract, Case Reports