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  2. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    Klinefelter syndrome is not an inherited condition. The extra X chromosome comes from the mother in approximately 50% of the cases. Maternal age is the only known risk factor. Women at 40 years have a four-times-higher risk of a child with Klinefelter syndrome than women aged 24 years. [15] [35] [36]

  3. California governor signs bill making insurance companies pay ...

    www.aol.com/california-governor-signs-bill...

    The estimated average cost per IVF cycle is about $12,000, according to the American Society for Reproductive Medicine (ASMR). But gynecologist Karen Tang, M.D., previously told USA TODAY that it ...

  4. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.

  5. University of California, San Francisco Fetal Treatment Center

    en.wikipedia.org/wiki/University_of_California...

    The Fetal Treatment Center at the University of California, San Francisco is a multidisciplinary care center dedicated to the diagnosis, treatment, and long-term follow-up of fetal birth defects. It combines the talents of specialists in pediatric surgery , genetics, obstetrics / perinatology , radiology , nursing , and neonatal medicine.

  6. Sertoli cell-only syndrome - Wikipedia

    en.wikipedia.org/wiki/Sertoli_cell-only_syndrome

    Sertoli cell-only syndrome (SCOS), also known as germ cell aplasia, is defined by azoospermia where the testicular seminiferous tubules are lined solely with sertoli cells. [2] Sertoli cells contribute to the formation of the blood-testis barrier and aid in sperm generation.

  7. XXXXY syndrome - Wikipedia

    en.wikipedia.org/wiki/XXXXY_syndrome

    XXXXY syndrome, also known as 49,XXXXY syndrome or Fraccaro syndrome, is an extremely rare aneuploidic sex chromosomal abnormality. It occurs in approximately 1 out of 85,000 to 100,000 males. [1] [2] [3] This syndrome is the result of maternal non-disjunction during both meiosis I and II. [4]

  8. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    Turner syndrome results from a single X chromosome (45,X or 45,X0). Klinefelter syndrome, the most common male chromosomal disease, otherwise known as 47,XXY, is caused by an extra X chromosome. Edwards syndrome is caused by trisomy (three copies) of chromosome 18. Down syndrome, a common chromosomal disease, is caused by trisomy of chromosome 21.

  9. File:Klinefelters Syndrome age diagnosis-en.svg - Wikipedia

    en.wikipedia.org/wiki/File:Klinefelters_Syndrome...

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