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Summary Of: XX gonadal dysgenesis

Thus XX gonadal dysgenesis is also referred to as... Familial cases of XX gonadal dysgenesis are on record... The XX gonadal dysgenesis is the related to the... In contrast XX gonadal dysgenesis has a normal female chromosome situation... Another type of XX gonadal dysgenesis is known as 46 xx gonadal dysgenesis epibulbar dermoid... XX gonadal dysgenesis with epibulbar dermoid...

Encyclodia Page On: XX gonadal dysgenesis

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OMIM | MeSH | hypogonadism | puberty | karyotype | FSH | LH | Estrogen | progesterone | Turner syndrome | Swyer syndrome | FSH-receptor | atresia | puberty | 1951 | sex hormones | estrogens | androgens | secondary sex characteristics | menstrual periods | adrenal glands | delayed puberty | gonadotropins | karyotype | estrogen | progestin | eggs | embryo transfer | Swyer syndrome | Turner syndrome | Gonadal dysgenesis | doi | NIH | Rare Diseases | v | Pathology | chromosome abnormalities | Q90-Q99 | 758 | Autosomal | Trisomies | Down syndrome | 21 | Edwards syndrome | 18 | Patau syndrome | 13 | Trisomy 9 | Warkany syndrome 2 | 8 | Trisomy 22 | Cat eye syndrome | 22 | Trisomy 16 | Monosomies | deletions | Wolf-Hirschhorn syndrome | 4 | Cri du chat | 5 | Williams syndrome | 7 | Jacobsen syndrome | 11 | Miller-Dieker syndrome | Smith-Magenis syndrome | 17 | 22q11.2 deletion syndrome | 22 | genomic imprinting | Angelman syndrome | Prader-Willi syndrome | 15 | X | Y | Monosomy | Turner syndrome (XO) | Trisomy | Tetrasomy | other karyotypes | Klinefelter's syndrome (47,XXY) | 48,XXYY | 49,XXXXY | Triple X syndrome (47,XXX) | 48,XXXX | 49,XXXXX | 47,XYY | Translocations | leukemia | lymphoma | Philadelphia chromosome | Burkitt's lymphoma | Anaplastic large cell lymphoma | Follicular lymphoma | Mantle cell lymphoma | Ewing's sarcoma | Gonadal dysgenesis | Mixed gonadal dysgenesis | Fragile X syndrome | Uniparental disomy | Categories | Gynecology | Genetic disorders |
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