tay-sachs
/ˈteɪ ˈsæks/Tradução: Doença genética hereditária do metabolismo de lipídios, mais comum em pessoas de ascendência judaica ashkenazi do Leste Europeu, na qual o acúmulo de lipídios no tecido nervoso causa deterioração neurológica progressiva e morte na primeira infância.
noun
/ˈteɪ ˈsæks/
Наследственное нарушение липидного обмена, наиболее часто встречающееся у лиц еврейского происхождения из Восточной Европы, при котором накопление липидов в нервной ткани приводит к смерти в раннем детстве.
Enfermedad hereditaria del metabolismo de los lípidos, más frecuente en personas de ascendencia judía de Europa del Este, en la que la acumulación de lípidos en el tejido nervioso provoca la muerte en la primera infancia.
Maladie héréditaire du métabolisme des lipides, la plus fréquente chez les personnes d'origine juive d'Europe de l'Est, où l'accumulation de lipides dans le tissu nerveux entraîne la mort dans la petite enfance.
Erbliche Stoffwechselstörung, bei der sich Lipide im Nervengewebe ansammeln und meist zum Tod im frühen Kindesalter führt; tritt besonders bei Juden osteuropäischer Herkunft auf.
Doença genética hereditária do metabolismo de lipídios, mais comum em pessoas de ascendência judaica ashkenazi do Leste Europeu, na qual o acúmulo de lipídios no tecido nervoso causa deterioração neurológica progressiva e morte na primeira infância.
一种遗传性脂质代谢障碍，最常见于东欧犹太裔人群，因神经组织中脂质蓄积而导致幼儿期死亡。
اضطراب وراثي في استقلاب الدهون (الغانغليوزيدات) يؤدي إلى تراكمها في الخلايا العصبية، ويظهر غالبًا عند اليهود الشرقيين، ويؤدي عادة إلى الوفاة في سن مبكرة.
A hereditary disorder of lipid metabolism, most frequently occurring in individuals of Jewish descent from eastern Europe, where accumulation of lipids in nervous tissue results in death in early childhood.
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Hereditary metabolic disorderC2formalmedical
A rare, inherited condition that causes progressive damage to nerve cells in the brain and spinal cord, typically leading to death in early childhood. It is most common among certain populations, including Ashkenazi Jews.
Наследственное метаболическое расстройствоEnfermedad de Tay-SachsMaladie de Tay-SachsHereditäre StoffwechselerkrankungDoença de Tay-Sachs遗传性代谢障碍اضطراب استقلابي وراثي- Tay-Sachs disease is caused by a deficiency of the enzyme hexosaminidase A.
- Infants with Tay-Sachs appear normal at birth but begin to show symptoms around six months of age.
- Genetic testing can identify carriers of the Tay-Sachs mutation.
Sinônimostay-sachs disease
- tay-sachs plural form
- tay-sachs' possessive plural form
- tay-sachs's possessive singular form