Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2004-7-5
pubmed:abstractText
Testicular cancer can impair spermatogenesis. In addition, chemotherapy or radiotherapy used for its treatment further damage testicular function mainly affecting highly proliferating germ cells. The multifaceted etiology of male infertility includes, among others, alterations of male reproductive tract differentiation such as monolateral or bilateral congenital absence of vas deferens and perturbations in adrenal steroid synthesis on a genetic basis such as 21beta-hydroxylase deficiency. Herein, we report the case of a male patient with primary infertility, probably related to a combination of genetic and acquired factors with different expressions over time.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0391-4097
pubmed:author
pubmed:issnType
Print
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
370-4
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:15233559-17-alpha-Hydroxyprogesterone, pubmed-meshheading:15233559-Adrenal Hyperplasia, Congenital, pubmed-meshheading:15233559-Adult, pubmed-meshheading:15233559-Carcinoma in Situ, pubmed-meshheading:15233559-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:15233559-Dehydroepiandrosterone Sulfate, pubmed-meshheading:15233559-Dexamethasone, pubmed-meshheading:15233559-Follicle Stimulating Hormone, pubmed-meshheading:15233559-Glucocorticoids, pubmed-meshheading:15233559-Humans, pubmed-meshheading:15233559-Male, pubmed-meshheading:15233559-Mutation, pubmed-meshheading:15233559-Obesity, pubmed-meshheading:15233559-Oligospermia, pubmed-meshheading:15233559-Steroid 21-Hydroxylase, pubmed-meshheading:15233559-Testicular Neoplasms, pubmed-meshheading:15233559-Testosterone, pubmed-meshheading:15233559-Vas Deferens
pubmed:year
2004
pubmed:articleTitle
Bilateral carcinoma in situ of the testis and cystic fibrosis transmembrane conductance regulator (CFTR) mutation in an azoospermic patient with late-onset 21beta-hydroxylase deficiency.
pubmed:affiliation
DiSEM, Cattedra di Endocrinologia, University of Genoa, Italy. luca.foppiani@hsanmartino.liguria.it
pubmed:publicationType
Journal Article, Case Reports