Any condition where one has muscle disorders (please note this is not a full exhaustive list but of more common conditions where one has acquired the condition rather than those discovered at birth or a young age, a specialist will conduct further tests for rare conditions)?
Rhabdomyolysis (Crush syndrome)
Pre-menstural syndrome (PMS) or Pre-menstural tension(PMT) (females only)
Acromegaly
Arthritis
Amyloidosis
Becker muscular dystrophy
Bell’s palsy (Facial Palsy)
Cataplexy (sudden loss of muscle tone while a person is awake leads to weakness and a loss of voluntary muscle control. It is often triggered by sudden, strong emotions such as laughter, fear, anger, stress, or excitement)
Cold-related injuries
Dermatomyositis/Juvenile Dermatomyositis
Fibromyalgia
Muscle Atrophy/low tone/wasting (including feeding difficulties)
Myoclonus (quick, involuntary muscle jerks)
Myositis
Myotonia congenita (muscular appearance)
Duchenne muscular dystrophy variety
Ehlers-Danlos
Erdheim-Chester disease
Emery-Dreifuss maculary dystrophy
Facioscapulohumeral Muscular Dystrophy (decrease in the ability to lift the arms due to weakness of muscles)
Fukuyama type congenital muscular dystrophy (mainly affect Japanese persons)
Frontotemporal Dementia (Pick’s disease)
Growing pains
Hirayama disease (damage or compression to the spinal cord causing muscle loss and weakness initially forearms and hands mainly in young males)
Huntington disease
Inclusion-Body Myositis
Kernicterus (to much bilirubin)
Lewy Body Dementia
Limb-Girdle dystrophy
Metabolic acidosis
Metabolic alkalosis
Mixed cryoglobulinemia (triggered by the cold)
Oculopharyngeal Muscle Conditions
Polymayalgia rheumatica
Polymyositis
Tendonitis
Orbital Myositis (idiopathic orbital or ocular myositis)
Phenylketonuria
Polymyositis
Lysosomal Lipid Storage and/or Lysosomal Lipid Metabolism Disorders and/or Mucopolysaccharides Metabolism Disorders (Mucopolysaccharidoses)
Mitochondrial Myopathy/Encephalomyopathy
Sarcoidosis
Scleroderma (Crest syndrome)
Trismus
Wernicke encephalopathy
Alpers Disease (childhood condition occurs from 3 months – 5 years old)
X-linked myopathy with excessive autophagy (especially weakness in legs)
Gastric Motility Conditions (Conditions Where The Movement Of Food In The Digestive System Is Affected)
Achalasia
Gastroparesis
Intussusception
Myotonic Dystrophy
Paralytic Ileus
Hirschsprung’s Disease
Dumping Syndrome
Other:
Syndromes related to muscle conditions?
Acute respiratory distress syndrome (affect lungs)
Newborn respiratory distress syndrome (affect lungs)
Compartment Syndrome
Rhabdomyolysis (Crush syndrome)
Angelman syndrome
Bartter’s syndrome/Gitelman syndrome (affects kidney, ear, muscles)
Coffin-Siris syndrome
Cornelia de Lange syndrome
Scleroderma (Crest syndrome)
DiGeorge syndrome
Dubowitz syndrome (narrow or triangle-shaped face with a high or sloping forehead, eczema, vision problems)
East syndrome (affect kidney, ear, movement)
Eosinophilia-myalgia syndrome (muscle pain and breathing problems, hair loss)
Felty syndrome
Gustavson syndrome
Kabuki syndrome
Klinefelter syndrome (male only)
Korsakoff Syndrome
Lambert-Eaton Syndrome
Marfan syndrome
Muscle Atrophy/low tone/wasting (including feeding difficulties) including syndromes causing this condition
Parsonage-Turner syndrome (Brachial plexus neuritis-is an uncommon neurological disorder characterised by rapid onset of severe pain in the shoulder and arm)
Prader-Willi syndrome
Pre-menstural syndrome (PMS) or Pre-menstural tension(PMT) (females only)
Myotonic dystrophy (Steinert disease, Ricker syndrome)
Post-Polio syndrome (caused by polio infection)
Rubinstein-Taybi syndrome
Russell-Silver syndrome
Smith Lemli Opitz syndrome
Sotos syndrome
Stiff Person Syndrome/Moersch-Woltmann Syndrome/ Isaacs Syndrome
Williams-Beuren syndrome
Wolfram syndrome
Wolf-Hirschhorn syndrome
Other: