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This article discusses about an inherited condition of the kidneys called Abderhalden – Kaufmann – Lignac Syndrome or Nephropathic Cystinosis . Nephropathic Cystinosis is an autosomal recessionary inherited disorder . The disease is do by accretion of amino acid cystine within the cells . Intracellular amino acid accumulation causes cellular damage . This usually affects major organ of the body , specificallykidneysandeyes . In this clause , we will talk over about the accumulation of cystine affecting the kidney and the result complication from them . The diseases often cause grave symptoms in infant and children.1This article will discuss the campaign , symptoms , and handling for Nephropathic Cystinosis . other diagnosing and treatment prevents early fateful complications.2
How Is Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis Defined?
Describe The Cause Of Cystinosis In Infants?
What Causes Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis?
What Is The Influence Of Gene Mutation In Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis?
Symptoms of Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
All the symptoms and signs of Falconi syndrome are note . Additional symptoms and signs are as follows-
Tests to Diagnose Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
Urine Examination
Blood Examination
Examination of Crystal-
Microbiology Studies for Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
Kidney Biopsy for Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
Radiological Studies for Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
Treatment for Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
Symptomatic Treatment For Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
Therapeutic Treatment For Abderhalden–Kaufmann–Lignac Syndrome or Nephropathic Cystinosis
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