20718196

Source:http://linkedlifedata.com/resource/pubmed/id/20718196

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004096, umls-concept:C0018553
pubmed:issue	3
pubmed:dateCreated	2010-8-19
pubmed:abstractText	Cowden's syndrome (CS) is a rare autosomal dominant disorder characterized by multiple hamartomas and an increased risk of breast, thyroid and endometrial carcinomas. Mutations of tumor suppressor gene PTEN (phosphatase and tensin homolog) on chromosome 10p23.2, which encodes a lipid phosphatase mediating cell cycle arrest and apoptosis, were first described in CS. Some studies have also implicated PTEN in the pathogenesis of bronchial asthma. Herein, we describe a boy with CS referred to the pediatric allergy unit with bronchial asthma symptoms. This patient is one of the very few reported cases with CS with lung disease and possibly the first with bronchial asthma.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0417505
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0041-4301
pubmed:author	pubmed-author:AlanayYaseminY, pubmed-author:KalayciOmerO, pubmed-author:OzsürekciYaseminY, pubmed-author:UtineGülen EdaGE, pubmed-author:YavuzSüleyman TolgaST
pubmed:issnType	Print
pubmed:volume	52
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	330-2
pubmed:meshHeading	pubmed-meshheading:20718196-Asthma, pubmed-meshheading:20718196-Child, pubmed-meshheading:20718196-Hamartoma Syndrome, Multiple, pubmed-meshheading:20718196-Humans, pubmed-meshheading:20718196-Male
pubmed:articleTitle	Cowden syndrome with bronchial asthma.
pubmed:affiliation	Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
pubmed:publicationType	Journal Article, Case Reports