منابع مشابه
The XXXXY sex chromosome abnormality.
The most common sex chromosome complex in sex chromatin-positive males with Klinefelter's syndrome is XXY. When the complex is XXYY or XXXY, the clinical findings do not seem to differ materially from those seen in XXY subjects, although more patients with these intersexual chromosome complements need to be studied to establish possible phenotypical expressions of the chromosomal variants.Two m...
متن کاملRare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes.
49,XXXXY and 48,XXXY syndromes are rare gonosomal aneuploidies in which the affected individuals present with characteristic facial and skeletal malformations, intrauterine growth retardation, and psychomotor retardation. Psychological, endocrinologic and orthopedic disorders constitute the major problems in the clinical follow-up. Sex chromosome abnormalities should especially be kept in mind ...
متن کاملParental decisions of prenatally detected sex chromosome abnormality.
Because of the widespread use of amniocentesis, the prenatal recognition of sex chromosome abnormality (SCA) has become increasingly common. Recent literature provided an insight into the understanding of the natural history and prognosis for individuals with SCA. Our study was designed to review the parental decision on pregnancy with SCA. Over the last 10 yr, we diagnosed 38 cases (0.50%) wit...
متن کاملSex chromosome abnormality in a patient with transsexualism.
Transsexualism, defined as the wish to change anatomical sex (Benjamin, 1954), is a psychosexual disorder usually not associated with physical abnormalities (Randell, 1970) or abnormality of the sex chromosomes (Money, 1963). In males with Klinefelter's syndrome, where there is an additional X chromosome, cases have been described with coincidental transsexualism (Money, 1963) and transvestism ...
متن کاملA Boy with Xxxxy Sex Chromosomes.
Eight patients with XXXXY sex chromosomes are on record (Fraccaro, Kaijser, and Lindsten, I960; Miller, Breg, Schmickel, and Tretter, I96I; Fraser, Boyd, Lennox, and Dennison, I96I; Fraccaro, Klinger, and Schutt, I962; Barr, Carr, Pozsonyi, Wilson, Dunn, Jacobson, and Miller, I962; Pfeiffer, I962; Schade, Sch6ller, and T6berg, I963). In addition two similar patients with a mosaic pattern have b...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1966
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.41.215.82