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38 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis

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

  • Hydronephrosis

    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] High association with other congenital anomalies such as imperforate anus, cardiac problems, Turner Syndrome, VACTERL association, cerebral and lumbo- sacral abnormalities[adc.bmj.com]

  • Mulibrey Nanism Syndrome

    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] […] disease in the right kidney, such as poor corticomedullary differentiation and cortical atrophy that were confirmed by renal scintigraphy (Fig. 3 ).[academic.oup.com] TownesBrocks Syndrome 14 Diabetes Insipidus 136 TreacherCollins Syndrome 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner[books.google.de]

  • Congenital Hydronephrosis

    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] High association with other congenital anomalies such as imperforate anus, cardiac problems, Turner Syndrome, VACTERL association, cerebral and lumbo- sacral abnormalities[adc.bmj.com]

  • Congenital Hypothyroidism without Goiter

    dysgenesis Enlarged kidney Aniridia Male pseudohermaphroditism Gonadoblastoma Ambiguous genitalia, male Diffuse mesangial sclerosis Ambiguous genitalia, female Prolonged[mendelian.co] syndrome: relation to hormone replacement therapy and karyotype‏ HH Elsedfy, RT Hamza, MH Farghaly, MS Ghazy ‏ Journal of Pediatric Endocrinology and Metabolism 25 (5-6),[scholar.google.com.eg] Dysgenesis, XY Type, with Associated Anomalies Gordon Syndrome Gorlin Chaudhry Moss Syndrome Grant Syndrome Growth Deficiency and Mental Retardation with Facial Dysmorphism[rgd.mcw.edu]

  • Mazabraud Syndrome

    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] Denys - Drash syndrome • Gonadal Dysgenesis • Diffuse mesangial sclerosis • Wilms tumour 56.[de.slideshare.net]

  • Ataxia Telangiectasia

    Certain endocrine abnormalities (eg, gonadal dysgenesis, testicular atrophy, diabetes mellitus) may occur.[msdmanuals.com] Cellular immunity can also be affected in A-T: abnormal development of the thymus, with absence of Hassall's corpuscles and corticomedullary differentiation, impaired delayed[err.ersjournals.com] Also, the impairment of cell cycle control can cause malformations, such as gonadal dysgenesis, which is found in patients with A-T.[ncbi.nlm.nih.gov]

  • Osteopetrosis

    dysgenesis ) GnRHR ( Gonadotropin-releasing hormone insensitivity ) EDNRB ( ABCD syndrome, Waardenburg syndrome 4a, Hirschsprung's disease 2 ) AVPR2 ( Nephrogenic diabetes[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] […] hypothyroidism 1 ) LHCGR ( Luteinizing hormone insensitivity, Leydig cell hypoplasia, Male-limited precocious puberty ) FSHR ( Follicle-stimulating hormone insensitivity, XX gonadal[en.wikipedia.org]

  • Waters-West Syndrome

    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] Return to top MALE GU SEX DISORDERS: GENETIC SEX TURNER SYNDROME : XO genotype. MIXED GONADAL DYSGENESIS : 1 defined gonad plus a contralateral streak gonad.[kumc.edu]

  • Meckel Syndrome

    Individuals with MGS may also exhibit microphthalmia, cleft lip, micrognathia, liver fibrosis, gonadal dysgenesis, and congenital cardiovascular malformations such as aortic[symptoma.com] […] appears to be failed interaction of the metanephric duct and renal blastema; the kidneys, therefore, show little corticomedullary differentiation, and the nephrons are severely[pathologyoutlines.com] syndrome ターナー症候群 HenryHubert Turner(1892 - 1970) American endocrinologist Tuttle タットル Tuttle test タットル試験 Tyndall チンダル Tyndall phenomenon チンダル現象 Tyrode タイロード Tyrode's solution[jams.med.or.jp]

  • Senior-Løken Syndrome

    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] Denys - Drash syndrome • Gonadal Dysgenesis • Diffuse mesangial sclerosis • Wilms tumour 56.[de.slideshare.net]

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