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27 Possible Causes for Abnormal Corticomedullary Differentiation, Diabetes Insipidus, female gonadal dysgenesis

Did you mean: Abnormal Corticomedullary Differentiation, Diabetes Insipidus, female, gonadal dysgenesis

  • Hydronephrosis

    ., diabetes insipidus, psychogenic polydipsia) Hydronephrosis of infection: due to bacterial toxins inhibiting smooth muscle contraction of the renal pelvis and ureter Pediatric[unboundmedicine.com] In Gardner-Silengo-Wachtel syndrome (Micrognathia, low set ears, double outlet right ventricle with VSD and 46 XY Gonadal dysgenesis). No polydactyly.[omicsonline.org] Perinephric urinoma Keyhole sign Loss of renal parenchyma, as suggested by: (i) cortical thinning, (ii) poor corticomedullary differentiation, (iii) increased renal echogenicity[indianpediatrics.net]

  • Fanconi Renotubular Syndrome

    Diabetes insipidus is also a rare complication of ifosfamide-induced renal disease.[ncbi.nlm.nih.gov] dysgenesis, trisomy X * Thymus in DiGeorge syndrome * Labia majora in popliteal pterygium syndrome * Corpus callosum, connecting the two sides of the brain, in Agenesis of[dbpedia.org] Abdominal ultrasound showed kidneys measuring 146 mm with preserved corticomedullary differentiation and no signs of hydronephrosis.[revistanefrologia.com]

  • Mulibrey Nanism Syndrome

    Insipidus 136 TreacherCollins Syndrome 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner Syndrome 17 Hermaphroditism[books.google.de] […] disease in the right kidney, such as poor corticomedullary differentiation and cortical atrophy that were confirmed by renal scintigraphy (Fig. 3 ).[academic.oup.com] Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18 Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism[books.google.de]

  • Senior-Løken Syndrome

    One individual had a mutlti-year history of diabetes insipidus and vision ‘problems’ before being diagnosed. Easy fatigability can be a chief complaint.[wohproject.org] dysgenesis NR0B1 300473 2-4 gonadal dysgenesis NR0B1 300473 2-4 NR5A1 480000 2-4 sex differentiation - SRY 480000 2-4 SRY 480000 2-4 Shaheen syndrome COG6 606977 2-4 Short[bioscientia.de] 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]

  • CAMFAK Syndrome

    insipidus archives any disease s symptoms. shingles herpes zoster symptoms complications and treatment .[300blackbroth.com] Chromosomal Trisomy 21, Turner’s syndrome, trisomy 13–15, trisomy 16–18, deletion chromosome 5 b.[iovs.arvojournals.org] […] renal corticomedullary differentiation High palate Camptodactyly Dolichocephaly Arachnodactyly High, narrow palate Renal hypoplasia Joint contracture of the hand Trophic[mendelian.co]

  • Tumor Lysis Syndrome

    Dehydration brought about by nausea, vomiting, diarrhea, and diabetes insipidus are commonly caused by the underlying malignancy and chemotherapy, resulting in low urine flow[flipper.diff.org] Another common feature of Turner syndrome is the failure of the ovaries to develop properly (gonadal dysgenesis).[rarediseases.org] The ultrasonographic image on the right shows a kidney from a patient with the tumor lysis syndrome, in which there is loss of the normal corticomedullary differentiation[ncbi.nlm.nih.gov]

  • Osteopetrosis

    insipidus 1) PTGER2 (Aspirin-induced asthma) Class B PTH1R (Jansen's metaphyseal chondrodysplasia) Class C CASR (Familial hypocalciuric hypercalcemia) Class F FZD4 (Familial[en.wikipedia.org] Normal corticomedullary differentiation was evident in five (P   0.06) and 12 (P   0.005) patients at 6 and 12 months, respectively.[ncbi.nlm.nih.gov] dysgenesis) GnRHR (Gonadotropin-releasing hormone insensitivity) EDNRB (ABCD syndrome, Waardenburg syndrome 4a, Hirschsprung's disease 2) AVPR2 (Nephrogenic diabetes insipidus[en.wikipedia.org]

  • Posterior Fusion of Lumbosacral Vertebrae-Blepharoptosis Syndrome

    insipidus Vasovagal syncope Vasquez Hurst Sotos syndrome VATER association Ve-Vh Vein of Galen aneurysmal malformations (VGAM) Vein of Galen aneurysmal dilatation (VGAD)[bioreference.net] , 45,X/46,XX or XY Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome Q96.8 Other variants of Turner's syndrome Q96.9 Turner's syndrome, unspecified Q97[embryology.med.unsw.edu.au] corticomedullary differentiation Occipital meningocele Dilated fourth ventricle Hepatic steatosis Tubulointerstitial fibrosis Tubular atrophy Undetectable electroretinogram[mendelian.co]

  • Waters-West Syndrome

    insipidus, nephrogenic ( AQP2) Diabetes insipidus, nephrogenic ( AVPR2) Diabetes insipidus, neurohypophyseal ( AVP) Diabetes mellitus type II ( AKT2) Diabetes mellitus, gestational[en.praenatal-medizin.de] Turner syndrome: Turner syndrome, Macro, autopsy (73731) Turner syndrome, Macro, autopsy (73732) Turner syndrome, Macro, autopsy (73733) Turner syndrome, Macro, autopsy ([atlases.muni.cz] […] atrophy Adrenal insufficiency Absence of renal corticomedullary differentiation Hemolytic anemia Ptosis Lethargy Pachygyria Heterotopia Decreased liver function Aspiration[mendelian.co]

  • Mazabraud Syndrome

    insipidus Fatal infant form of LCH Fever Anemia Rash Hepatosplenomegaly BPOP Rare Hands & feet Rapid growth Cellular cartilage, bizarre fibroblasts, disorganized Fibrous[cram.com] Effects of recombinant human growth hormone on height in Turner syndrome .; 生长激素对Turner综合征的促身高作用 3.[dictall.com] differentiation, being replaced classically by a homogeneous ground glass appearance, although mixed lucencies and sclerosis are also common 2-4.[radiopaedia.org]

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