Linked Life Data

20467695

Source:http://linkedlifedata.com/resource/pubmed/id/20467695

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2010-5-14
pubmed:abstractText
Albright's hereditary osteodystrophy includes an heterogeneous group of genetic diseases, including the pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism. Features of this disease are: round faces, over-weight, subcutaneous calcifications and brachydactylia. Pseudohypoparathyroidism type Ia is associated with laboratory abnormalities such as hypocalcemia, and hyperphosphatemia due to parathormone resistance. Furthermore, these patients may present peripheral resistance to other hormones, such as gonadotrophins and thyroids. Pseudo-pseudohypoparathyroidism has no peripheral resistance to these hormones. We present three patients evaluated in our hospital with clinical manifestations of Albright's syndrome.
pubmed:language
spa
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1668-3501
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
108
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e24-7
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
[Albright's hereditary osteodystrophy: report of three cases].
pubmed:affiliation
Servicio de Dermatología, Hospital de Pediatría Prof. Dr. Juan P. Garrahan. mariambujan@yahoo.com
pubmed:publicationType
Journal Article, English Abstract, Case Reports