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13 Possible Causes for Intermittent Slow Activity, Muscle Weakness, Round Face

  • Cushing Syndrome

    The clinical sign indicative for CS leading to referral to the endocrinologist was muscle weakness in the man and plethora in the woman.[] Symptoms include a round face, thin arms and legs, severe fatigue and muscle weakness, high blood pressure and high blood sugar, purple or pink stretch marks on the skin,[] 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[]

  • Hyponatremia

    A 52-year-old Sri Lankan man presented with anorexia, nausea, fatigue, generalized muscle weakness, and cramps for 1 week.[] Renina: hiperaldosteronism I ii scazuta, II crescuta HTA A 34-year-old Caucasian female presents with truncal obesity, a rounded "moon face", and a "buffalo hump".[] Other symptoms include: Fatigue Convulsions Headache Muscle weakness or spasms Nausea and vomiting Restlessness Confusion Decreased consciousness Treatment of Hyponatremia[]

  • Hypocalcemia

    A 73-year-old man with metastatic melanoma presented to the Emergency Department for the chief complaints of imbalance, general muscle weakness, abdominal pain and tingling[] Round face. Short neck. Shortening of the metacarpals and metatarsals. Hypothyroidism. Diabetes mellitus. Gonadal dysgenesis.[] Symptoms include numbness and/or tingling of the hands, feet, or lips, muscle cramps, muscle spasms, seizures, facial twitching, muscle weakness, lightheadedness, and slow[]

  • Fibromyalgia

    Besides variable proximal muscle weakness, myotonia, and precocious cataracts, muscle pain and stiffness are prominent presenting features of DM2.[] A 39-year-old woman with a 3-year history of a rounded face developed widespread myalgia.[] […] temporal focal θ slowing and excessive β.[]

  • Propionic Acidemia

    Clinical presentation was with acute aphasia, generalized hypotonia, and muscle weakness.[] It’s not detailed enough to round with 1. Open or select the patient(s) you want 2.[] N Engl J Med 292: 491496 16 Walk D et al. (1994) Intermittent encephalopathy, reversible nerve conduction slowing, and MRI evidence of cerebral white matter disease in methylene-tetrahydrofolate[]

  • Hereditary Hyperekplexia

    weakness.[] The disease has_symptom large joints, has_symptom wide set eyes, has_symptom round flat face.[] Occasionally EEG recording shows nonspecific temporal theta activity or bilateral runs of polyspike-slow waves followed by brief flattening of background activity(10,11).[]

  • Early Infantile Epileptic Encephalopathy Type 6

    Low muscle tone is often present, which can manifest as muscle weakness.[] The results from the two rounds of consultation were consolidated and validated through an Advisory Board face to face meeting with eight clinical experts that took place[] Sometimes a diffuse or unilateral slowing of the background if they are recorded after a prolonged seizure.[]

  • Locked-in Syndrome

    Deterioration of nerve tissue and muscle wastage cause progressive muscle weakness as the condition develops.[] His face lolled to one side but if he said something funny or noteworthy, he would wait for the interpreter to translate it then snap his head round to offer me a smile.[] The EEG may be normal or may show slight slowing, with slow activity record intermittently especially theta activity on ‘awake’ EEG.[]

  • AMACR Deficiency

    These episodes were associated with myalgia, muscle weakness, and high creatinine kinase (CK) levels, up to 58,000 U/L (normal 47–222 U/L).[] Contributions from many leading surgical pathologists give you well-rounded, expert answers to any question that you may face.[] EEG showed excess slow activity with intermittent episodes of delta waves in the frontotemporal regions, independently over both hemispheres.[]

  • Wolf-Hirschhorn Syndrome

    Muscle weakness (hypotonia) is common. The palate is sometimes cleft. Everyone with this diagnosis suffers from a developmental disability which is most often severe.[] The main clinical features are short stature, round face with short philtrum, palpebral ptosis and large ears with detached pinnae.[] The stereotypic electroclinical pattern of WHS is described as intermittent bursts of 2-3 Hz high voltage slow waves with superimposed spike and spike wave activity in centroparietal[]

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