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The results should NOT be considered a diagnosis.
Please consult your health care provider.
edit important variables such as:
demo: duration, demo: age, difficulty speaking, impaired sensations in foot (feet), muscle weakness in foot (feet), stiff neck, palpitations
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Swimmer's shoulder - shoulder pain in competitive swimmer
a.k.a Impingement syndrome, painful arc syndrome, supraspinatus syndrome, thrower's shoulder
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Polyneuropathy - disorder of multiple peripheral nerves
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Trauma neck - neck injury
'trauma neck' is considered a medical emergency
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Neurosyphilis - syphilis infection that involves the central nervous system
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Multiple endocrine neoplasia type 2b - disease affecting multiple endocrine glands
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Syringomyelia - damage to spinal cord by progressively enlarging cavity in its center
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Syphilis - multisystem chronic STD
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syphilis
cardiac, female reproductive system-gynecological, infectious diseases, male reproductive system, neurology, dermatology
[chronic with acute exacerbation]
blister(s) or bump(s) in genital area in females, lump or swelling in groin in females, lump or swelling in groin in males, poor coordination
Syphilis is a sexually transmitted disease (STD) caused by a spirochaete bacterium, Treponema pallidum. Syphilis has many alternate names, including "syph", "Cupid's Disease", "the Pox" (or "great pox", to distinguish it from smallpox), "lues" (hence luiphobia, or fear of syphilis), and the "French disease.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Homocystinuria - multisystem metabolic disease due to abnormal methionine metabolism
a.k.a Cystathionine beta synthase deficiency
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homocystinuria
cardiovascular, genetic or congenital, hematological, metabolic, muscles, musculoskeletal and connective tissue disorders, neurological
[chronic]
anemia, curvature of spine, delayed development, pain in leg(s)
Homocystinuria, also known as Cystathionine beta synthase deficiency, is an inherited disorder of the metabolism of the amino acid methionine. It is an inherited autosomal recessive trait, which means a child needs to inherit the defective gene from both parents to be affected.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Osteogenesis imperfecta type I - genetic bone disease causing frequent fractures
a.k.a Brittle Bone Disease, Lobstein syndrome
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Osteogenesis imperfecta types III and IV - genetic bone disease
a.k.a Brittle Bone Disease, Lobstein syndrome
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Known synonyms for your symptoms:
• increased joint mobility -
hyperextensible joints , hypermobile joints , can bend joints backwards , very flexible joints , increased range of motion of joints , excessive mobility of joints , joint mobility increased , joint mobility excessive , increased joint laxity , increased mobility elbow , increased mobility wrist , increased mobility hip , increased mobility knee , increased mobility ankle , increased mobility fingers or thumbs , increased mobility toes
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