Create issue ticket

2,809 Possible Causes for Abnormal Corticomedullary Differentiation, Blood Urea Nitrogen Increased, Retinal Degeneration

  • Senior Loken Syndrome

    blood urea nitrogen * Increased blood creatinine level * Thickening of kidney filtration tissues * Endstage kidney disease * Polyuria * Enuresis * Inability to concentrate[checkorphan.org] […] diagnosis of these varieties of hereditary tapeto-retinal degeneration.[ncbi.nlm.nih.gov] Absence of renal corticomedullary differentiation Short proximal phalanx of finger Vascular ring Aplasia of the middle phalanx of the hand Pyelonephritis Frontal upsweep[mendelian.co]

  • Mucopolysaccharidosis

    degeneration Hearing impairment – Deafness Musculoskeletal disease – Short stature; joint stiffness; symptoms of peripheral nerve entrapment Findings from examination may[emedicine.medscape.com] Retinal degeneration may occur, but the cornea usually remains clear. Appearance is normal at birth with excessive growth taking place during first two years of life.[icd9data.com] Corneal clouding was mentioned as another symptom characteristic of MPS and may be associated with glaucoma, retinal degeneration, and optic nerve swelling with subsequent[symptoma.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Mucopolysaccharidosis 2

    Typical signs and symptoms include: Hearing impairment Joint stiffness Coarse face Upper airway disease Carpal tunnel syndrome Communicating hydrocephalus Retinal degeneration[symptoma.com] Retinal degeneration is seen to a lesser degree in MPS IIB. Patients diagnosed with MPS IIB can live beyond the fifth decade of life.[emedicine.medscape.com] Retinal degeneration may occur, but the cornea usually remains clear. Appearance is normal at birth with excessive growth taking place during first two years of life.[icd10data.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Nephronophthisis 1

    blood urea nitrogen (BUN), isosthenuria, and negative response to Pitressin.[healio.com] Mutations in AHI1, which encodes a cilium-localized protein, have been shown to cause a form of Joubert syndrome that is highly penetrant for retinal degeneration.[ncbi.nlm.nih.gov] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov]

  • Nephronophthisis 3

    blood urea nitrogen (BUN), isosthenuria, and negative response to Pitressin.[healio.com] […] coworkers2 was called by them: "a retinal dystrophy undistlnguishable from Leber's tapeto retinal degeneration."[healio.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov]

  • Nephronophthisis 2

    blood urea nitrogen (BUN), isosthenuria, and negative response to Pitressin.[healio.com] Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov]

  • Nephronophthisis 9

    blood urea nitrogen (BUN), isosthenuria, and negative response to Pitressin.[healio.com] Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov]

  • Nephronophthisis 12

    blood urea nitrogen (BUN), isosthenuria, and negative response to Pitressin.[healio.com] Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov]

  • Nephronophthisis 13

    blood urea nitrogen (BUN), isosthenuria, and negative response to Pitressin.[healio.com] Pigmentosa Primary Cilium Retinal Degeneration Situs Inversus Cystic Kidney Nephronophthisis (NPH) is an autosomal recessive inherited cystic kidney disorder.[ciliajournal.biomedcentral.com] Renal sonograms of all patients showed enlarged and echogenic kidneys that lacked corticomedullary differentiation.[ncbi.nlm.nih.gov]

  • Membranoproliferative Glomerulonephritis

    He was referred to the nephrology department due to abruptly increased levels of blood urea nitrogen (BUN; 68 mg/dL) and serum creatinine (sCr; 2.2 mg/dL).[kjim.org] A peripherin/retinal degeneration slow mutation (Pro-210- Arg) associated with macular and peripheral retinal degeneration. Ophthalmology. 1995;102(2):246-55. 7.[sboportal.org.br] […] as age-related macular degeneration.[ncbi.nlm.nih.gov]

    Missing: Abnormal Corticomedullary Differentiation

Similar symptoms