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241 Possible Causes for Brandt Syndrome, Hypothyroidism

  • Zinc Deficiency

    It’s thought that hair loss due to hypothyroidism will not improve unless a zinc supplement is taken along with the thyroid drugs. 5.[doctorshealthpress.com] It is also called acrodermatitis enteropathy, primary zinc malabsorption syndrome , Danbolt-Closs syndrome and Brandt syndrome .[dermnetnz.org] It is also called acrodermatitis enteropathy, primary zinc malabsorption syndrome, Danbolt-Closs syndrome and Brandt syndrome.[dermnetnz.org]

  • Iron Deficiency

    Iron deficiency slows your body's thyroid function and blocks its metabolism-boosting effects, according to the National Academy of Hypothyroidism.[huffpost.com] Brandt SJ, Bodine DM, Dunbar CE, Nienhuis AW. Dysregulated interleukin 6 expression produces a syndrome resembling Castleman’s disease in mice.[ncbi.nlm.nih.gov] […] have an underactive thyroid url: text: Iron deficiency slows your body's thyroid function and blocks its metabolism-boosting effects, according to the National Academy of Hypothyroidism[abcnews.go.com]

  • Lower Gastrointestinal Hemorrhage

    Brandt, Bloody diarrhea in an elderly patient, Gastroenterology, 128, 1, (157), (2005).[dx.doi.org] Georges Coremans, Cilansetron: a novel, high-affinity 5-HT3receptor antagonist for irritable bowel syndrome with diarrhea predominance, Therapy, 2, 4, (559), (2005).[dx.doi.org]

  • Turner Syndrome

    Three girls from that subgroup were euthyroid, 5 had subclinical hypothyroidism, and 3 were diagnosed with overt hypothyroidism.[ncbi.nlm.nih.gov] Brandt, P. E. Warburton and L.[doi.org] […] in Turner syndrome, [6] obtain thyroid function tests at diagnosis; repeat TSH measurements every 1-2 years or if symptoms develop, because hypothyroidism may develop at[emedicine.medscape.com]

  • Down Syndrome

    Among the subclinical hypothyroidism group, 25 (73.5%) had transient hypothyroidism and 9 (26.5%) persistent hypothyroidism.[ncbi.nlm.nih.gov] BRITA RYDE BRANDT, Impaired tactual perception in children with Down's syndrome, Scandinavian Journal of Psychology, 37, 3, (312), (1996).[dx.doi.org] Clinicians should be aware of the increased risk of gallstones in hypothyroid children with DS, even in neonatal age.[ncbi.nlm.nih.gov]

  • Pseudohypoparathyroidism

    The case is of interest as the child on serial follow-up over a period of 2 years developed hypothyroidism.[ncbi.nlm.nih.gov] Acrodysostosis syndromes. BoneKEy Rep. 225, 1–7 (2012). 133. Ablow, R. C., Hsia, Y. E. & Brandt, I. K.[nature.com] She also had hypothyroidism which is known to utilize the G protein pathway. She developed T 1 diabetes mellitus (T1DM) while under follow-up.[ncbi.nlm.nih.gov]

  • Velocardiofacial Syndrome

    […] results of this study combined with the information in the literature on the main defects in VCFS (palatal abnormalities, cardiac anomalies, thymic hypoplasia or aplasia, hypothyroidism[ncbi.nlm.nih.gov] […] surgery for congenital cardiac abnormalities Thymus transplant for thymus absence Cleft palate repair Vitamin D and calcium supplements for hypocalcemia associated with hypothyroidism[syndromespedia.com] Hypothyroidism is uncommon, but screening is part of the work-up for short stature. Renal anomalies occur in a third of patients.[clinicaladvisor.com]

  • Young-Simpson Syndrome

    This rare genetic disorder is characterized by congenital hypothyroidism, mental retardation and blepharophimosis.[ncbi.nlm.nih.gov] Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome).[doi.org] Larson, Congenital Hypothyroidism, Pediatric Endocrinology, 10.1007/978-1-60761-395-4_15, (261-273), (2013).[doi.org]

  • Congenital Macroglossia

    Congenital hypothyroidism presenting as isolated macroglossia in a term neonate: A case report. Indian Journal of Child Health, 5 (3), 225-227. Retrieved from[atharvapub.net] G. syndrome and carbohydrate metabolism. Lancet 1969 I , 374. Google Scholar 4. Combs, J. T., J. A. Grunt , and J. K. Brandt : New syndrome of neonatal hypoglycemia.[link.springer.com] […] examination, the following signs may be present: Macroglossia and coarse facial features Hypotonia Large anterior fontanelle Umbilical hernia Slow development Goiter Pallor Myxedema[lecturio.com]

  • Bangstad Syndrome

    […] and acanthosis nigricans, small teeth, prognathism, dislocated radial heads without generalized skeletal dysplasia, however, tall vertebrae, moderate mental retardation, hypothyroidism[en.wikipedia.org] Brandt J, Wong C, Mihm S, Roberts J, Smith J, Brewer E, et al. Invasive pneumococcal disease and hemolytic uremic syndrome. Pediatrics. 2002;110:371–6.[springermedizin.de] Wong CS, Mooney JC, Brandt JR, Staples AO, Jelacic S, Boster DR, et al.[springermedizin.de]

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