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Sepiapterin reductase deficiency is an inh … Sepiapterin reductase deficiency is an inherited pediatric disorder characterized by movement problems, and most commonly displayed as a pattern of involuntary sustained muscle contractions known as dystonia. Symptoms are usually present within the first year of age, but diagnosis is delayed due to physicians lack of awareness and the specialized diagnostic procedures. Individuals with this disorder also have delayed motor skills development including sitting, crawling, and need assistance when walking. Additional symptoms of this disorder include intellectual disability, excessive sleeping, mood swings, and an abnormally small head size. SR deficiency is a very rare condition. The first case was diagnosed in 2001, and since then there have been approximately 30 reported cases. At this time, the condition seems to be treatable, but the lack of overall awareness and the need for a series of atypical procedures used to diagnose this condition pose a dilemma.to diagnose this condition pose a dilemma.
, Недостаточность сепиаптеринредуктазы — заб … Недостаточность сепиаптеринредуктазы — заболевание, вызываемое нарушением работы фермента , участвующего в цепочке синтеза тетрагидробиоптерина. Развивающаяся при этом заболевании недостаточность тетрагидробиоптерина вызывает снижение уровней нейромедиатора дофамина, вследствие чего у пациентов отмечаются двигательные нарушения, такие как дистония и окулогирные кризы.я, такие как дистония и окулогирные кризы.
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Недостаточность сепиаптеринредуктазы — заб … Недостаточность сепиаптеринредуктазы — заболевание, вызываемое нарушением работы фермента , участвующего в цепочке синтеза тетрагидробиоптерина. Развивающаяся при этом заболевании недостаточность тетрагидробиоптерина вызывает снижение уровней нейромедиатора дофамина, вследствие чего у пациентов отмечаются двигательные нарушения, такие как дистония и окулогирные кризы.я, такие как дистония и окулогирные кризы.
, Sepiapterin reductase deficiency is an inh … Sepiapterin reductase deficiency is an inherited pediatric disorder characterized by movement problems, and most commonly displayed as a pattern of involuntary sustained muscle contractions known as dystonia. Symptoms are usually present within the first year of age, but diagnosis is delayed due to physicians lack of awareness and the specialized diagnostic procedures. Individuals with this disorder also have delayed motor skills development including sitting, crawling, and need assistance when walking. Additional symptoms of this disorder include intellectual disability, excessive sleeping, mood swings, and an abnormally small head size. SR deficiency is a very rare condition. The first case was diagnosed in 2001, and since then there have been approximately 30 reported cases. At this timproximately 30 reported cases. At this tim
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rdfs:label |
Sepiapterin reductase deficiency
, Недостаточность сепиаптеринредуктазы
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