|
arthrogryposis multiplex congenita +
Axial Myopathy, Late-Onset +
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts
bilirubin metabolic disorder +
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia
Carey-Fineman-Ziter syndrome +
Chanarin-Dorfman syndrome +
Congenital Myopathy with Neuropathy and Deafness
Congenital Universal Muscular Hypoplasia of Krabbe
Craniomandibular Disorders +
Ehlers-Danlos syndrome kyphoscoliotic type 2
eosinophilia-myalgia syndrome
Erythrocyte Amp Deaminase Deficiency
Erythrocyte Lactate Transporter Defect
Extravasation of Diagnostic and Therapeutic Materials
familial periodic paralysis +
Femoracetabular Impingement
Fingerprint Body Myopathy
Gamstorp-Wohlfart syndrome
Granulovacuolar Lobular Myopathy with Electrical Myotonia
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis
Heterotopic Ossification +
Hypertrophia Musculorum Vera
Internal Anal Sphincter Myopathy
Intraoperative Complications +
Kocher-Debre-Semelaigne Syndrome
Late-Onset Carnitine Palmitoyltransferase II Deficiency
Long Term Adverse Effects
Marinesco-Sjogren syndrome
Medial Tibial Stress Syndrome
Menstruation Disturbances +
Mitochondrial DNA Depletion Syndrome, Myopathic Form +
Muscle Weakness + A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251)
myofascial pain syndrome +
Myopathic Carnitine Deficiency
Myopathy with Lactic Acidosis, Hereditary
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Pathological Protein Aggregation
Pectoralis Muscle, Absence of
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss
Postoperative Complications +
Proximal Myopathy with Focal Depletion of Mitochondria
Singleton Merten Syndrome +
Skeletal Muscle Reperfusion Injury
systemic primary carnitine deficiency disease
Tel Hashomer Camptodactyly Syndrome
Treft Sanborn Carey Syndrome
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy
Uruguay faciocardiomusculoskeletal syndrome
very long chain acyl-CoA dehydrogenase deficiency
|
|