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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, weakness, swollen joint(s), pain in several joints, limitation of movement, poor appetite
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Osteoarthritis - type of arthritis seen in the elderly
a.k.a OA, degenerative arthritis, degenerative joint disease
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Osteochondroma - benign bone tumor
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Renal osteodystrophy - bone problems caused by renal disease
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Celiac disease - malabsorption resulting from abnormal reaction to gliadin
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Malabsorption - defect in absorption of nutrients from the bowel
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Neurofibromatosis type 1 - inherited condition with lumps in multiple areas and dark spots on skin
a.k.a Neurofibromatosis Type I, von Recklinghausen disease, NF-1
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neurofibromatosis type 1
genetic or congenital, neurology, dermatology
[chronic with acute exacerbation]
blister(s) or bump(s) on back, lump(s) in skin, pelvic pain in females, poor coordination
Neurofibromatosis type I (NF-1), also known as von Recklinghausen syndrome, comprises, along with neurofibromatosis type II (a.k.a. MISME syndrome), tuberous sclerosis, Sturge-Weber, and Von Hippel-Lindau disease, the phakomatoses or neurocutaneous syndromes, all of which have both neurologic and dermatologic lesions.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Short bowel syndrome - malabsortion caused by decreased length of small bowel
a.k.a SBS, short gut syndrome, simply short gut
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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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Hypophosphatasia - rare inherited metabolic disease resulting in decreased bone mineralization
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McCune-Albright Syndrome - genetic disease with bone, pigmentation and hormonal problems
a.k.a polyostotic fibrous dysplasia
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Known synonyms for your symptoms:
• bowed limbs -
bowed leg(s) , curved limbs , crooked limbs , curved extremities , crooked extremities , extremities bowed , extremities curved , extremities crooked , arms or legs curved , arms or legs crooked , arms or legs bowed , limbs bowed , limbs crooked , limbs curved
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