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'''49,XXYYY syndrome''' is a [[intersex]] [[CTM]]/[[AMAB|DMAB]] variation. It's featured with facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age and moderate intellectual disability.<ref>[https://pubmed.ncbi.nlm.nih.gov/8330452/]</ref> Tissues sampled for chromosome studies of external [[Ambiguous Genitalia|ambiguous genitalia]] and abdominal gonads, consisting of a left [[Ovotesticular|ovotestis]] and a right primitive testis, contained cells 46,XX, 47,[[XYY Syndrome|XXY]] and 49,XXYYY sex chromosomes.<ref>[https://www.karger.com/Article/PDF/129719][https://pubmed.ncbi.nlm.nih.gov/13959068/][https://op.europa.eu/en/publication-detail/-/publication/b7a528a6-2d20-4384-9e52-38579a0f3677]</ref> |
'''49,XXYYY syndrome''' is a [[intersex]] [[CTM]]/[[AMAB|DMAB]] variation. It's featured with facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age and moderate intellectual disability.<ref>[https://pubmed.ncbi.nlm.nih.gov/8330452/]</ref> Tissues sampled for chromosome studies of external [[Ambiguous Genitalia|ambiguous genitalia]] and abdominal gonads, consisting of a left [[Ovotesticular|ovotestis]] and a right primitive testis, contained cells 46,XX, 47,[[XYY Syndrome|XXY]] and 49,XXYYY sex chromosomes.<ref>[https://www.karger.com/Article/PDF/129719][https://pubmed.ncbi.nlm.nih.gov/13959068/][https://op.europa.eu/en/publication-detail/-/publication/b7a528a6-2d20-4384-9e52-38579a0f3677]</ref> |
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[[Category:Intersex Traits]] |
[[Category:Intersex Traits]] |
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[[Category:Terminology]] |
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Revision as of 22:43, 10 May 2021
49,XXYYY syndrome is a intersex CTM/DMAB variation. It's featured with facial dysmorphism, mild microcephaly, limitation of supination at the elbows, delayed bone age and moderate intellectual disability.[1] Tissues sampled for chromosome studies of external ambiguous genitalia and abdominal gonads, consisting of a left ovotestis and a right primitive testis, contained cells 46,XX, 47,XXY and 49,XXYYY sex chromosomes.[2]