Results 31 to 40 of about 208,465 (197)
Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis. [PDF]
Congenital hypothyroidism (CH) is a frequent neonatal endocrine disease with an incidence of about 1:2500 worldwide. Although thyroid dysgenesis (TD) is the most frequent cause of CH cases, its pathogenesis remains unclear. The aim of this study was to screen the hematopoietically-expressedhomeobox gene (HHEX) mutations in Chinese children with TD ...
Liu S +5 more
europepmc +3 more sources
Worldwide neonatal screening for congenital hypothyroidism (CH) is a gold standard of active surveillance in newborns. Prompt diagnosis, subsequent timely treatment implementation, and proper dosage of levothyroxine (L-T4) are crucial for normal growth ...
Elżbieta Lipska +6 more
doaj +1 more source
Advanced maternal age in Indian children with thyroid dysgenesis. [PDF]
A retrospective review of medical records of 80 children with thyroid dysgenesis (TD) was conducted to determine the association of gender and maternal age with TD. The study subjects were attending the Pediatric Endocrinology Clinic of our hospital which is a large tertiary care Multispecialty Pediatric Center located in Chandigarh, Northwest India ...
Dayal D +3 more
europepmc +4 more sources
Gene expression profiles during thyroid embryonic development [PDF]
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively known as thyroid dysgenesis. Defects in growth and/or differentiation of the thyroid primordium can result in an absent (athyreosis) or hypoplastic ...
Parrillo, Luca
core +1 more source
Thyroid dysgenesis (TD) is a major cause of primary congenital hypothyroidism; however, the molecular mechanism underlying this process is unclear.
Rui‐jia Zhang +6 more
doaj +1 more source
Permanent or Transient Congenital Hypothyroidism: A Diagnostic Dilemma. [PDF]
ABSTRACT Aim Distinguishing between transient congenital hypothyroidism (TCH) and permanent congenital hypothyroidism (PCH) remains clinically challenging and is typically deferred until the age of 2–3 years, to minimise the potential risk of adverse neurodevelopmental effects due to treatment cessation.
Dermitzaki N +4 more
europepmc +2 more sources
Lingual and Mediastinal Ectopic Thyroid with No Normal Thyroid Gland – A Very Rare Occurrence
Introduction Ectopic thyroid is a rare congenital condition. Dual ectopic thyroid is rarer still with only 30 cases reported in literature.
Shyam Kalyan N +3 more
doaj +3 more sources
The zebrafish model to identify new genes involved in thyroid development [PDF]
Thyroid organogenesis is a very complex developmental process that leads to the formation of an organ able to produce specific hormones through specification, migration, structural organization and functional differentiation of thyroid precursor cells ...
Porreca, Immacolata
core +1 more source
Age-related changes of prevalence of thyroid dysgenesis.
Age-related changes of prevalence of thyroid dysgenesis.
Hideki Hattori (7325933) +8 more
core +1 more source
Shining a Light on Hidden Thyroids: A Case Exploring the Potential of Technetium Imaging for Lingual Thyroid Diagnosis [PDF]
Ectopic thyroid, the presence of thyroid tissue in locations other than the normal anterior neck region between the second and fourth tracheal cartilages, is the most common form of thyroid dysgenesis.
Anbarasi Madoure +2 more
doaj +1 more source

