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2. Cystinosis - Wikipedia

   en.wikipedia.org/wiki/Cystinosis

   Without treatment, children with cystinosis are likely to experience complete kidney failure by about age ten. With treatment this may be delayed into the patients' teens or 20s. Other signs and symptoms that may occur in patients include muscle deterioration, blindness, inability to swallow, impaired sweating, decreased hair and skin ...

3. Autosomal dominant polycystic kidney disease - Wikipedia

   en.wikipedia.org/wiki/Autosomal_dominant...

   Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, life-threatening inherited human disorders and the most common hereditary kidney disease. [ 1 ] [ 2 ] It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and modifier genes ...

4. Nephronophthisis - Wikipedia

   en.wikipedia.org/wiki/Nephronophthisis

   Infantile, juvenile, and adolescent forms of nephronophthisis have been identified. Although the range of characterizations is broad, people affected by nephronophthisis typically present with polyuria (production of a large volume of urine), polydipsia (excessive liquid intake), and after several months to years, end-stage kidney disease, a condition necessitating either dialysis or a kidney ...

5. Alport syndrome - Wikipedia

   en.wikipedia.org/wiki/Alport_syndrome

   Alport syndrome is a genetic disorder [1] affecting around 1 in 5,000–10,000 children, [2] characterized by glomerulonephritis, end-stage kidney disease, and hearing loss. [3] Alport syndrome can also affect the eyes, though the changes do not usually affect vision, except when changes to the lens occur in later life.

6. Can Ozempic Actually Cause Hair Loss? - AOL

   www.aol.com/ozempic-actually-cause-hair-loss...

   Diseases like lupus and certain thyroid problems can also cause hair loss, as can stress, poor diet, and medications like chemotherapy drugs. Diabetes is just one of the conditions on that list.

7. Lesch–Nyhan syndrome - Wikipedia

   en.wikipedia.org/wiki/Lesch–Nyhan_syndrome

   The drug allopurinol is utilized to stop the conversion of oxypurines into uric acid, and prevent the development of subsequent arthritic tophi (produced after having chronic gout), kidney stones, and nephropathy, the resulting kidney disease. Allopurinol is taken orally, at a typical dose of 3–20 mg/kg per day.

8. Boy no longer has to travel for treatment thanks to father’s ...

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9. Gitelman syndrome - Wikipedia

   en.wikipedia.org/wiki/Gitelman_syndrome

   Gitelman syndrome (GS) is an autosomal recessive kidney tubule disorder characterized by low blood levels of potassium and magnesium, decreased excretion of calcium in the urine, and elevated blood pH. [2] It is the most frequent hereditary salt-losing tubulopathy. Gitelman syndrome is caused by disease-causing variants on both alleles of the ...