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1.
N Engl J Med ; 353(1): 58-63, 2005 Jul 07.
Article in English | MEDLINE | ID: mdl-15941849

ABSTRACT

Monozygotic 24-year-old twins presented with discordant ovarian function. One had had premature ovarian failure at the age of 14 years, whereas her sister had normal ovaries and three naturally conceived children. After unsuccessful egg-donation therapy, the sterile twin received a transplant of ovarian cortical tissue from her sister by means of a minilaparotomy. Within three months after transplantation, the recipient's cycles resumed and serum gonadotropin levels fell to the normal range. During the second cycle, she conceived, and her pregnancy progressed uneventfully. At 38 weeks' gestation, she delivered a healthy-appearing female infant.


Subject(s)
Diseases in Twins/surgery , Infertility, Female/surgery , Ovary/transplantation , Pregnancy , Primary Ovarian Insufficiency/surgery , Adult , Female , Humans , Infant, Newborn , Infertility, Female/etiology , Ovary/abnormalities , Ovary/cytology , Primary Ovarian Insufficiency/complications , Twins, Monozygotic
2.
Am J Med Genet A ; 116A(1): 77-9, 2003 Jan 01.
Article in English | MEDLINE | ID: mdl-12476456

ABSTRACT

We report the unusual finding of velocardiofacial syndrome (VCF) in an unexplained 46,XX male. A microdeletion of 22q11.2 was confirmed by fluorescence in situ hybridization (FISH) analysis. Routine G-banded chromosome analysis revealed an XX sex chromosome constitution. FISH was performed using the SRY probe and failed to detect hybridization. The sex chromosome status of the patient was further investigated by PCR testing to screen for the presence of 24 distinct loci spanning the Y chromosome. PCR screening failed to detect any apparent Y chromosome material.


Subject(s)
Abnormalities, Multiple/genetics , Chromosomes, Human, Y/genetics , Disorders of Sex Development , Face/abnormalities , Heart Defects, Congenital/pathology , Sex Chromosome Aberrations , Abnormalities, Multiple/pathology , Child , Chromosome Deletion , Chromosomes, Human, Pair 22/genetics , Cleft Palate/pathology , Humans , Male , Syndrome
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