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35 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis, Pediatric Disorder

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

  • 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] Disorders of mitochondrial energy metabolism may be a primary factor underlying tubular cell apoptosis in hydronephrosis.[ncbi.nlm.nih.gov] Perinephric urinoma Keyhole sign Loss of renal parenchyma, as suggested by: (i) cortical thinning, (ii) poor corticomedullary differentiation, (iii) increased renal echogenicity[indianpediatrics.net]

  • Ataxia Telangiectasia

    Certain endocrine abnormalities (eg, gonadal dysgenesis, testicular atrophy, diabetes mellitus) may occur.[msdmanuals.com] […] all neurosurgical conditions of infants, children and adolescents, with special expertise in the management of pediatric brain tumors, hydrocephalus, spinal cord disorders[massgeneral.org] 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]

  • Osteopetrosis

    dysgenesis) GnRHR (Gonadotropin-releasing hormone insensitivity) EDNRB (ABCD syndrome, Waardenburg syndrome 4a, Hirschsprung's disease 2) AVPR2 (Nephrogenic diabetes insipidus[en.wikipedia.org] Full Title: Follow-up of phase I/II study of CaspaCide T cells from an HLA-partially matched family donor after negative selection of TCR αβ T cells in pediatric patients[clinicaltrialsregister.eu] 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]

  • 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] […] in children Health Articles See all » Treatments for Pediatric Spinal Deformities Infrared Therapy: Health Benefits and Risks Everything You Need to Know About Giving Up[news-medical.net] […] 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]

  • Congenital Hemihypertrophy

    Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci.[richtlijnendatabase.nl] Bilateral adrenal pheochromocytomas have also been described in patients with Beckwith–Wiedemann syndrome (BWS), a pediatric overgrowth disorder, usually presenting with hemihypertrophy[edmcasereports.com] Heterogeneous Growth delay Respiratory distress Meningoencephalocele Episodic tachypnea Absence of renal corticomedullary differentiation Brainstem dysplasia Neonatal breathing[mendelian.co]

  • Tumor Lysis Syndrome

    Another common feature of Turner syndrome is the failure of the ovaries to develop properly (gonadal dysgenesis).[rarediseases.org] Author information 1 Department of Pediatrics, Sapporo Hokuyu Hospital, Higashi-Sapporo 6-6, Shiroishiku, Sapporo, 003-0006, Japan, d-suzuki@chashu.org.[ncbi.nlm.nih.gov] 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]

  • 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] […] with congenital and acquired kidney and urinary tract disorders that can cause hydronephrosis.[rush.edu] Perinephric urinoma Keyhole sign Loss of renal parenchyma, as suggested by: (i) cortical thinning, (ii) poor corticomedullary differentiation, (iii) increased renal echogenicity[indianpediatrics.net]

  • 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] Our proband is one of the rare examples of mulibrey nanism outside Finland and extends the mutation spectrum in this disorder. a Pediatric Gastroenterology Unit b Pediatric[journals.lww.com] […] disease in the right kidney, such as poor corticomedullary differentiation and cortical atrophy that were confirmed by renal scintigraphy (Fig. 3 ).[academic.oup.com]

  • 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] J Pediatr Endocrinol Metab. 2006; 19(suppl 2):577-582. (11.) Diaz A, Danon M, Crawford J. McCune-Albright syndrome and disorders due to activating mutations of GNAS1.[thefreelibrary.com] differentiation, being replaced classically by a homogeneous ground glass appearance, although mixed lucencies and sclerosis are also common 2-4.[radiopaedia.org]

  • Congenital Hypothyroidism without Goiter

    dysgenesis Enlarged kidney Aniridia Male pseudohermaphroditism Gonadoblastoma Ambiguous genitalia, male Diffuse mesangial sclerosis Ambiguous genitalia, female Prolonged[mendelian.co] You’ll benefit from unique, global perspectives on adult and pediatric endocrinology prepared by an international team of renowned authorities.[books.google.es] 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]

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