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searching for Congenital hypothyroidism 25 found (84 total)

alternate case: congenital hypothyroidism

Posterior fontanelle (95 words) [view diff] exact match in snippet view article find links to article

fontanelle is called lambda. A delay in closure is associated with congenital hypothyroidism. This article incorporates text in the public domain from page

FOXE1 (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 localization

Tenterfield 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 gene

PAX8 (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 development

Hypothyroidism 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. Primary

Sodium/iodide cotransporter (3,135 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 with

Iodotyrosine deiodinase (2,207 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 preventing

Dual 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. The

Spanish Water Dog (699 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 Originally

British 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, retrieved

Young–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"

Harbor–UCLA Medical Center (1,990 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 possible

Dual 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.

Gesell 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-up

Wu Sing-yung (1,006 words) [view diff] exact match in snippet view article find links to article

thyroid function marker (W-compound) that may help better manage congenital hypothyroidism. His Thyroid Laboratory at Long Beach VA Medical Center, in collaboration

Dianne Webster (667 words) [view diff] exact match in snippet view article find links to article

L Hofman (20 June 2012). "Etiology of increasing incidence of congenital hypothyroidism in New Zealand from 1993-2010". The Journal of Clinical Endocrinology

Jostel's TSH index (2,106 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 4629398

Jaundice (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 jaundice

Microlissencephaly (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 (5,790 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 asymptomatic

Genetic testing (6,621 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 have

Scott Rivkees (2,281 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 the

Sickle cell disease (14,947 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 (6,440 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-phosphate

List 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;