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189 Possible Causes for Delayed Bone Age, Muscle Weakness, Round Face

  • Mucopolysaccharidosis

    Compression of the cervical spinal cord, caused by glycosaminoglycan infiltration of the dura, may lead to spastic paresis if not corrected by neurosurgical intervention.[]

  • Vitamin D Deficiency

    Apart from the well-known effects on bone metabolism, this condition is also associated with muscle weakness, predominantly of the proximal muscle groups.[] NIWA provides a year round daily guide of the UV throughout New Zealand.[] She presented with fractures during the first year-of-life followed by bone deformities, delayed development, failure-to-thrive, and pneumonias.[]

  • Cushing's Disease

    Some symptoms are Upper body obesity Thin arms and legs Severe fatigue and muscle weakness High blood pressure High blood sugar Easy bruising Lab tests can show if you have[] A 39-year-old woman with a 3-year history of a rounded face developed widespread myalgia.[] Weak bones Extra fat around neck Acne Round face Balding (women) Fatigue Hip and shoulder weakness Poor concentration Swelling of feet/legs Menstrual irregularity Diabetes[]

  • Iatrogenic Cushing's Disease

    Potty belly due to muscle weakness, fat redistribution and water retention. Muscle weakness leads to instability in standing and walking.[] Signs and symptoms include a round face, upper body obesity, fragile and thin skin, purple stretch marks in the skin, fatigue, muscle weakness, hypertension, diabetes mellitus[] The indica ted treatment was topical with hydrocortisone acetate and delayed bone age (BA) (6 months BA for 1 year 3 months in chronological age).[]

  • Barth Syndrome

    Main symptoms: Heart muscle weakness (cardiomyopathy) Neutropenia (lack of white blood cells needed to fight bacterial infections) Fatigue and general muscle weakness Growth[] face with full cheeks, broad forehead, prominent chin, large ears and deep-set eyes What are the causes of Barth syndrome?[] bone age exercise intolerance skeletal muscle myopathy BTHS has an estimated prevalence of 1 in 300,000-400,000 live births.[]

  • Addison's Disease

    The physical examination was completely normal except for muscle weakness, hyperpigmentation on labial mucosa and skin in a patient.[] People with Cushing’s typically have a rounded “moon” face, gain weight around the trunk, and have slender arms and legs.[] Symptoms & Causes The most common symptoms are fatigue, muscle weakness, loss of appetite, weight loss, and abdominal pain.[]

  • Aarskog Syndrome

    […] presented with the uncommon finding of ophthalmoplegia and three previously unreported oral-facial findings: enamel dysplasia, a "col" deformity of the anterior mandible and a paresis[] The main findings are asynchronic and delayed bone age, shortened long tubular bones with wide metaphyses, brachyphalangy, hypoplasia of the middle phalanges of the fifth[] face with widow's peak and, in one of them, ptosis of the eyelids.[]

  • Schwartz-Jampel Syndrome

    554 Case 89A A Woman with Muscle Weakness and a Skin Rash 559 Case 90 A Man with Muscle Pains 567 Case 91 An Older Woman with Progressive Muscle Weakness 572 Case 92 An HIVInfected[] […] back [ more ] 0002808 Mask-like facies Expressionless face Lack of facial expression Mask-like facial appearance [ more ] 0000298 Micrognathia Little lower jaw Small jaw[] "Schwartz-Jampel syndrome (SJS) is a rare genetic disorder characterized by abnormalities of the skeletal muscles, including muscle weakness and stiffness (myotonic myopathy[]

  • Zellweger Syndrome

    The symptoms of adrenal insufficiency include tiredness, loss of appetite and muscle weakness.[] face Circular face Round facial appearance Round facial shape [ more ] 0000311 Single transverse palmar crease 0000954 Subependymal cysts 0002416 Talipes equinovarus Club[] Direct involvement of muscle mitochondria in this disease may interfere with energy metabolism and contribute to the clinical findings of hypotonia, weakness, and respiratory[]

  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    The individual experiences this as muscle weakness or paralysis. For more information about Anderson-Tawil Syndrome click here .[] Additional facial features include a round (bulbous) nose, a thin upper lip, a triangular-shaped face, highly-arched roof of the mouth (palate), a cleft palate, and underdevelopment[] Muscle strength usually returns to normal between episodes. However, mild muscle weakness may eventually become permanent.[]

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