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3,073 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis, Immunoglobulin M Decreased

Did you mean: Abnormal Corticomedullary Differentiation, female, gonadal dysgenesis, Immunoglobulin M Decreased

  • 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]

  • Celiac Disease

    syndrome, Williams syndrome, selective immunoglobulin (Ig)A deficiency and first degree relatives of individuals with celiac disease.[ncbi.nlm.nih.gov] […] dental enamel defects, osteoporosis, short stature, delayed puberty and persistent iron deficiency anemia and in asymptomatic individuals with type 1 diabetes, Down syndrome, Turner[ncbi.nlm.nih.gov]

    Missing: Abnormal Corticomedullary Differentiation
  • Childhood Celiac Disease

    syndrome Williams syndrome A relative with celiac disease[gikids.org] Turner Syndrome and Celiac Disease: A Case-Control Study. Pediatrics. 2016 Feb. 137 (2):e20152232. [Medline]. Osterweil N.[emedicine.medscape.com] syndrome and selective IgA deficiency, as well as those with first-degree relatives with CD.[glutenfreetherapeutics.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Malignant Melanoma

    Syndrome 03 Oct 1995 Ed Jennings Cleared of All Charges 13 Sep 1995 Genentech Completes Negotiations, Purchases Land For New Manufacturing Facility in Vacaville, CA 21 Aug[gene.com] Earnings for Third Quarter 1995 05 Oct 1995 Genentech's Blood Platelet Factor (TPO) Enters the Clinic as Phase I Trial Begins 04 Oct 1995 Genentech Submits NDA for Nutropin in Turner's[gene.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Hypogammaglobulinemia

    Serum immunoglobulin determination at Walter Reed General Hospital revealed an immunoglobulin G level of 150 mg per 100 ml and absence of immunoglobulins A and M.[pubs.rsna.org] Celiac Disease and Turner Syndrome. J Pediatric Gastroenterol Nutr. 1998 May; 26(5): 496-9. 3.Stenberg AE, et al.[eposters.net] dysgenesis ) GnRHR ( Gonadotropin-releasing hormone insensitivity ) EDNRB ( ABCD syndrome, Waardenburg syndrome 4a, Hirschsprung's disease 2 ) AVPR2 ( Nephrogenic diabetes[en.wikipedia.org]

    Missing: Abnormal Corticomedullary Differentiation
  • Persistent Polyclonal B-cell Lymphocytosis

    dysgenesis syndrome Lupus erythematosus panniculitis Lupus erythematosus profundus Lupus erythematosus tumidus Luteal-phase-dependent febrile episode Luteal-phase-dependent[orpha.net] ’s syndrome and dorsal kyphoscoliosis.[medtextfree.wordpress.com] […] spina bifida aperta Lumbosacral spina bifida cystica Lunatomalacia Lundberg syndrome Lung agenesis-heart defect-thumb anomalies syndrome Lung fibrosis-immunodeficiency-46,XX gonadal[orpha.net]

    Missing: Abnormal Corticomedullary Differentiation
  • Common Variable Immunodeficiency

    […] serum levels of immunoglobulin G (IgG) and immunoglobulin A (IgA) are characteristic of the disorder, about 50% of CVID patients also have decreased immunoglobulin M (IgM[medigoo.com] These include Bloom syndrome, Fanconi anemia, trisomy 21, Turner syndrome, short-limbed skeletal dysplasia, cartilage-hair hypoplasia, Shwachman syndrome and ectodermal dysplasia[hawaii.edu] Although decreased serum levels of immunoglobulin G (IgG) and immunoglobulin A (IgA) are characteristic, approximately 50% of patients with the deficiency also have diminished[emedicine.medscape.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Congenital Agammaglobulinemia

    Claes-Jensen type syndromic X-linked intellectual disability Siderius type syndromic X-linked intellectual disability Snyder type transient hypogammaglobulinemia Wilson-Turner[rgd.mcw.edu] syndrome Wiskott-Aldrich syndrome X-linked adrenal hypoplasia congenita X-linked chondrodysplasia punctata 1 X-linked chronic granulomatous disease X-linked cone-rod dystrophy[rgd.mcw.edu]

    Missing: Abnormal Corticomedullary Differentiation
  • Premature Ovarian Failure

    Antibodies against thyroglobulin, nuclear antigens, heart, tissue gluten, or increased levels of immunoglobulin (Ig)M, or decreased levels of complement C3 and C4 were significantly[ncbi.nlm.nih.gov] Thus, even in Turner’s Syndrome (45,XO), or classic gonadal dysgenesis, some patients have been known to undergo spontaneous puberty and even onset of early menses prior to[fcionline.com] Physical exam of patients with suspected ovarian failure should look for characteristic features of Turner syndrome (see chapter on Turner Syndrome) (i.e., short stature,[clinicaladvisor.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Skin Cancer

    Javascript er ikke aktivert i din nettleser. Dette er nødvendig for å bruke Oncolex. Kontakt din systemadministrator for å aktivere JavaScript. Medical editor Åse Bratland MD Oncologist Oslo University Hospital Recently updated 09.03.2013 Skin cancer is divided into: Malignant melanoma - originating from melanocytes in[…][oncolex.org]

    Missing: Abnormal Corticomedullary Differentiation female gonadal dysgenesis

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