Puruckherr Michael, Pooyan Payam, Girish Mirle R, Byrd Ryland P, Roy Thomas M
James H. Quillen Veterans Affairs Medical Center 111-B, PO Box 4000, Mountain Home, TN 37684-4000, USA.
Sleep Med. 2004 Jul;5(4):379-81. doi: 10.1016/j.sleep.2003.12.006.
Acid maltase deficiency (AMD) is a rare autosomal recessive genetic disorder that results in an accumulation of glycogen in the lysosomal storage vacuoles. It is classified as a glycogen storage disease (type II) and is also known as Pompe's disease. The prognosis of the patient with AMD is poor and the main cause of death is respiratory failure. We report a female patient whose respiratory insufficiency was documented to occur most severely during rapid eye movement sleep and who benefited clinically from the institution of nocturnal noninvasive bilevel positive airway pressure.
酸性麦芽糖酶缺乏症(AMD)是一种罕见的常染色体隐性遗传疾病,可导致糖原在溶酶体储存泡中蓄积。它被归类为糖原贮积病(II型),也被称为庞贝氏病。AMD患者的预后较差,主要死因是呼吸衰竭。我们报告了一名女性患者,其呼吸功能不全在快速眼动睡眠期间最为严重,夜间采用无创双水平气道正压通气治疗后临床症状得到改善。