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Find link is a tool written by Edward Betts.searching for Congenital hypothyroidism 25 found (82 total)
alternate case: congenital hypothyroidism
Posterior fontanelle
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fontanelle is called lambda. A delay in closure is associated with congenital hypothyroidism. This article incorporates text in the public domain from pageFOXE1 (1,006 words) [view diff] exact match in snippet view article find links to article
gene cause Bamforth-Lazarus syndrome and are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis. The map localizationTenterfield Terrier (510 words) [view diff] exact match in snippet view article find links to article
one of the then-Miniature Fox Terrier clubs. A study looking at congenital hypothyroidism in the Tenterfield Terrier found a mutation in the R593W genePAX8 (2,314 words) [view diff] exact match in snippet view article find links to article
interact with NK2 homeobox 1. The PAX8 gene is also associated congenital hypothyroidism due to thyroid dysgenesis because of its role in growth and developmentSodium/iodide cotransporter (3,133 words) [view diff] exact match in snippet view article find links to article
PMID 2249482. Albero R, Cerdan A, Sanchez Franco F (December 1987). "Congenital hypothyroidism from complete iodide transport defect: long-term evolution withHypothyroidism in dogs (4,319 words) [view diff] no match in snippet view article find links to article
most common endocrinopathies in dogs. It is either acquired or congenital. Hypothyroidism is classified as either primary, secondary, or tertiary. PrimaryIodotyrosine deiodinase (2,204 words) [view diff] exact match in snippet view article find links to article
effectively. In some countries, newborn babies are tested for congenital hypothyroidism and treated immediately if the disease is detected, safely preventingDual oxidase 2 (1,901 words) [view diff] exact match in snippet view article find links to article
biosynthesis of thyroid hormones, supported by the discovery of congenital hypothyroidism resultant from an inactivating mutation in the DUOX2 gene. TheSpanish Water Dog (704 words) [view diff] exact match in snippet view article find links to article
disease) Exocrine pancreatic insufficiency Allergies Cataracts Congenital hypothyroidism with goitre (CHG) Distichia Cherry eye Neuroaxonal dystrophy OriginallyBritish Thyroid Foundation (551 words) [view diff] case mismatch in snippet view article find links to article
- NHS". www.nhs.uk. Retrieved 29 November 2022. Childhood and Congenital Hypothyroidism Patient UK "EMIS Health", Wikipedia, 8 September 2022, retrievedYoung–Simpson syndrome (1,078 words) [view diff] exact match in snippet view article find links to article
"Young-Simpson syndrome: further delineation of a distinct syndrome with congenital hypothyroidism, congenital heart defects, facial dysmorphism, and mental retardation"Action Medical Research (1,143 words) [view diff] exact match in snippet view article find links to article
adopted in UK hospitals). Helping develop routine screening for congenital hypothyroidism (CHT – a thyroid disorder in newborn babies) which was introducedDual oxidase 1 (2,137 words) [view diff] exact match in snippet view article find links to article
"Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism". N. Engl. J. Med. 347 (2): 95–102. doi:10.1056/NEJMoa012752.Harbor–UCLA Medical Center (1,982 words) [view diff] exact match in snippet view article find links to article
develop a simple, highly effective newborn screening test for congenital hypothyroidism, including developing the micro assay methods that made it possibleJostel's TSH index (1,714 words) [view diff] exact match in snippet view article find links to article
Chatterjee, VK; Dattani, MT (2015). "Recent advances in central congenital hypothyroidism". J Endocrinol. 227 (3): R51-71. doi:10.1530/JOE-15-0341. PMC 4629398Gesell Developmental Schedules (1,555 words) [view diff] exact match in snippet view article find links to article
Long-term consequences of the early treatment of children with congenital hypothyroidism detected by neonatal screening in Nanjing, Chine: A 12-year follow-upWu Sing-yung (967 words) [view diff] exact match in snippet view article find links to article
function marker (W-compound) that may help to better management of congenital hypothyroidism. His Thyroid Laboratory at Long Beach VA Medical Center, in collaborationJaundice (5,109 words) [view diff] exact match in snippet view article find links to article
cholestasis Pyknocytosis (due to vitamin deficiency) Cretinism (congenital hypothyroidism) Sepsis or other infectious causes Transient neonatal jaundiceMicrolissencephaly (2,704 words) [view diff] exact match in snippet view article find links to article
Marwaha, Ram Kumar (2013-11-01). "Lissencephaly presenting with congenital hypothyroidism". Journal of Pediatric Endocrinology and Metabolism. 26 (11–12):Thyroid hormones (5,787 words) [view diff] exact match in snippet view article find links to article
hormone availability for the foetus and its developing brain. Congenital hypothyroidism occurs in every 1 in 1600–3400 newborns with most being born asymptomaticGenetic testing (6,424 words) [view diff] exact match in snippet view article find links to article
genetic disorder that causes mental illness if left untreated) and congenital hypothyroidism (a disorder of the thyroid gland). People with PKU do not haveScott Rivkees (2,272 words) [view diff] case mismatch in snippet view article find links to article
combined. While at Indiana University, Rivkees initiated the Indiana Congenital Hypothyroidism Follow-up Program. While in Connecticut he was appointed to theSickle cell disease (15,276 words) [view diff] exact match in snippet view article find links to article
metropolitan France, ahead of phenylketonuria (one in 10,862), congenital hypothyroidism (one in 3,132), congenital adrenal hyperplasia (one in 19,008)Genetic studies on Arabs (6,358 words) [view diff] exact match in snippet view article find links to article
Interventions after birth, including: newborn biochemical screening for congenital hypothyroidism, phenylketonuria (PKU), galactosaemia, sickle cell disorder, glucose-6-phosphateList of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article
ketosis-prone; 612227; PAX4 Diabetes mellitus, neonatal, with congenital hypothyroidism; 610199; GLIS3 Diabetes mellitus, noninsulin-dependent; 125853;