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1.
Genet Mol Res ; 4(4): 755-9, 2005 Dec 30.
Article in English | MEDLINE | ID: mdl-16475122

ABSTRACT

The live birth of a triploidy infant is a very rare event and death usually occurs within the first hours of life. Triploid cases with a survival of more than two months are infrequent. We report on an infant with a 69,XXX chromosome constitution who survived 164 days. Chromosomal analysis demonstrated a 69,XXX karyotype with no evidence of mosaicism. This is the longest survival reported for this condition to date in Greece and the fourth longest worldwide. The infant was admitted to our clinic several times due to respiratory problems, and supplementary oxygen was required. The improved survival of our case was possibly due to better management of respiratory illness and prematurity, and these are essential factors that physicians should consider carefully with such rare cases.


Subject(s)
Abnormalities, Multiple/genetics , Longevity , Polyploidy , Sex Chromosome Aberrations , Abnormalities, Multiple/diagnosis , Fatal Outcome , Female , Greece , Humans , Infant, Newborn
2.
Ann Genet ; 47(2): 185-90, 2004.
Article in English | MEDLINE | ID: mdl-15183752

ABSTRACT

46,XY pure gonadal dysgenesis, first described in 1955 by Swyer, results from testicular tissue loss during the first 8 weeks of fetal life, a critical period for male differentiation. We describe a case of an 18 years old patient presented to us with a chief complain of primary amenorrhea. Chromosomal analysis revealed a 46,XY karyotype. A molecular investigation was undertaken in an attempt to determine mutations in SRY and AR genes through DNA sequencing. Mutations were shown to be absent. The molecular basis of Swyer syndrome is still unknown, although the presence of mutations in testicular organizing genes downstream of SRY is still to rule out. The patient, who is considered as female, was placed on estrogen replacement therapy, while bilateral prophylactic laparoscopic gonadectomy was programmed due to the high prevalence of gonadal tumors in this syndrome. No signs of malignance were detected in the gonadal tissue, which predicts that an intact SRY gene is usually, but not always, not related to the formation of malignancies like dysgeminomas or gonadoblastomas.


Subject(s)
Chromosome Aberrations , Genes, sry , Gonadal Dysgenesis, 46,XY/genetics , Mosaicism , Receptors, Androgen/genetics , Adolescent , Female , Humans
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