UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 筋力低下患者へのアプローチapproach to the patient with muscle weakness [show details]
… metabolic myopathy. However, many metabolic myopathies have a slowly progressive rather than episodic course. Medication, alcohol, or substance-abuse may be a clue to drug-induced myopathy. Endocrinopathy …
- 2. 代謝性ミオパチーへのアプローチapproach to the metabolic myopathies [show details]
…signs, and laboratory abnormalities resulting from a metabolic myopathy vary with the underlying defect. Most patients with a metabolic myopathy (eg, glycogen storage diseases, carnitine palmitoyltransferase …
- 3. 全身性疾患のミオパシーmyopathies of systemic disease [show details]
…muscle may become affected. The diagnosis of such a myopathy may be more difficult if it is the presenting manifestation of the endocrinopathy. Muscle disease is a common complication of congenital and adult-onset …
- 4. 薬物誘導性ミオパシーdrug induced myopathies [show details]
… unknown, drug-induced myopathy is among the most common causes of muscle disease. Drug-induced myopathy ranges from mild myalgias with or without mild weakness to chronic myopathy with severe weakness and …
- 5. 炎症性ミオパチーの病因pathogenesis of inflammatory myopathies [show details]
…inflammatory myopathies, including dermatomyositis (DM), polymyositis (PM), antisynthetase syndrome, immune-mediated necrotizing myopathy (IMNM), inclusion body myositis (IBM), and other myopathies and related …
Related Links
- (ネマリン杆状体ミオパチー) ●ネマリンミオパチー (NM) は, 筋力低下, 筋緊張低下, 深部腱反射低下または欠損が特徴である 筋力低下は通常, 顔, 頸部屈曲筋, 近位四肢筋で最も重度である ●臨床分類; 発症年齢と運動および呼吸器病変の重症度で6つの型がある
- 生まれながらに筋組織の形態に異常があり、そのため生後間もなく、あるいは幼少期から、「筋力が弱い」、「体が柔らかい」などの筋力低下に関わる症状を認める病気です。
- 遺伝的な筋肉の病気(筋疾患)の一つです。
★リンクテーブル★
[★]
- 英
- nemaline myopathy
- 同
- 杆状体ミオパチー rod body myopathy、先天性杆状体病 congenital rod disease
- 関
- 常染色体優性型ネマリンミオパチー
[★]
- 英
- body
- ラ
- corpus、corpora
- 関
- 肉体、身体、本体、コーパス、ボディー
[★]
- 英
- rod, rod shape of cell
- 関
- 杆体