Autosomal dominant Emery-Dreifuss muscular dystrophy
ORPHA:98853Etiological subtypeAutosomal dominantChildhood
Ассоциированные гены4
| Ген | Полное название | Тип связи | Тип гена | OMIM |
|---|---|---|---|---|
| LMNA | lamin A/C | Disease-causing germline mutation(s) in | gene with protein product | 150330 |
| SYNE1 | spectrin repeat containing nuclear envelope protein 1 | Disease-causing germline mutation(s) in | gene with protein product | 608441 |
| TMEM43 | transmembrane protein 43 | Disease-causing germline mutation(s) in | gene with protein product | 612048 |
| SYNE2 | spectrin repeat containing nuclear envelope protein 2 | Disease-causing germline mutation(s) in | gene with protein product | 608442 |
Фенотипы (HPO)44
Очень частый (80–99%)7
HP:0000767Pectus excavatum
HP:0001315Reduced tendon reflexes
HP:0001387Joint stiffness
HP:0002486Myotonia
HP:0003198Myopathy
HP:0003236Elevated circulating creatine kinase concentration
HP:0006785Limb-girdle muscular dystrophy
Частый (30–79%)20
HP:0000912Sprengel anomaly
HP:0001288Gait disturbance
HP:0001771Achilles tendon contracture
HP:0002155Hypertriglyceridemia
HP:0002515Waddling gait
HP:0002987Elbow flexion contracture
HP:0003141Increased LDL cholesterol concentration
HP:0003306Spinal rigidity
HP:0003418Back pain
HP:0003458EMG: myopathic abnormalities
HP:0003691Scapular winging
HP:0003805Rimmed vacuoles
HP:0004631Decreased cervical spine flexion due to contractures of posterior cervical muscles
HP:0008948Proximal upper limb amyotrophy
HP:0008956Proximal lower limb amyotrophy
HP:0008994Proximal muscle weakness in lower limbs
HP:0008997Proximal muscle weakness in upper limbs
HP:0011807Type 1 muscle fiber atrophy
HP:0030051Tip-toe gait
HP:0030117Absent muscle fiber emerin
Периодический (5–29%)11
HP:0000508Ptosis
HP:0001252Hypotonia
HP:0001513Obesity
HP:0001644Dilated cardiomyopathy
HP:0001678Atrioventricular block
HP:0002650Scoliosis
HP:0002808Kyphosis
HP:0003307Hyperlordosis
HP:0005115Supraventricular arrhythmia
HP:0008064Ichthyosis
HP:0009125Lipodystrophy
Очень редкий (1–4%)5
HP:0001605Vocal cord paralysis
HP:0001639Hypertrophic cardiomyopathy
HP:0001645Sudden cardiac death
HP:0002747Respiratory insufficiency due to muscle weakness
HP:0005155Ventricular escape rhythm
Исключён (0%)1
HP:0001249Intellectual disability
Лекарства и терапия
Источник: Open Targets Platform (в реальном времени)
Клинические исследования
Источник: ClinicalTrials.gov (в реальном времени)