{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T04:55:04Z","timestamp":1783486504205,"version":"3.55.0"},"reference-count":52,"publisher":"The Endocrine Society","issue":"9","license":[{"start":{"date-parts":[[2023,3,8]],"date-time":"2023-03-08T00:00:00Z","timestamp":1678233600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,8,18]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Introduction<\/jats:title>\n                  <jats:p>Congenital hypothyroidism with gland-in-situ (CH-GIS) is usually attributed to mutations in the genes involved in thyroid hormone production. The diagnostic yield of targeted next-generation sequencing (NGS) varied widely between studies. We hypothesized that the molecular yield of targeted NGS would depend on the severity of CH.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>Targeted NGS was performed in 103 CH-GIS patients from the French national screening program referred to the Reference Center for Rare Thyroid Diseases of Angers University Hospital. The custom targeted NGS panel contained 48 genes. Cases were classified as solved or probably solved depending on the known inheritance of the gene, the classification of the variants according to the American College of Medical Genetics and Genomics, the familial segregation, and published functional studies. Thyroid-stimulating hormone at CH screening and at diagnosis (TSHsc and TSHdg) and free T4 at diagnosis (FT4dg) were recorded.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>NGS identified 95 variants in 10 genes in 73 of the 103 patients, resulting in 25 solved cases and 18 probably solved cases. They were mainly due to mutations in the TG (n = 20) and TPO (n = 15) genes. The molecular yield was, respectively, 73% and 25% if TSHsc was \u2265 and &amp;lt; 80 mUI\/L, 60% and 30% if TSHdg was \u2265 and &amp;lt; 100 mUI\/L, and 69% and 29% if FT4dg was \u2264 and &amp;gt; 5 pmol\/L.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusion<\/jats:title>\n                  <jats:p>NGS in patients with CH-GIS in France found a molecular explanation in 42% of the cases, increasing to 70% when TSHsc was \u2265 80 mUI\/L or FT4dg was \u2264 5 pmol\/L.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1210\/clinem\/dgad119","type":"journal-article","created":{"date-parts":[[2023,3,8]],"date-time":"2023-03-08T19:36:39Z","timestamp":1678304199000},"page":"e779-e788","source":"Crossref","is-referenced-by-count":7,"title":["The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing"],"prefix":"10.1210","volume":"108","author":[{"given":"Lucie","family":"Levaillant","sequence":"first","affiliation":[{"name":"Department of Pediatric Endocrinology and Diabetology, University Hospital of Angers , 49000 Angers , France"},{"name":"Reference Center for Rare Diseases of Thyroid and Hormone Receptivity, University Hospital of Angers , 49000 Angers , France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Natacha","family":"Bouhours-Nouet","sequence":"additional","affiliation":[{"name":"Department of Pediatric Endocrinology and Diabetology, University Hospital of Angers , 49000 Angers , France"},{"name":"Reference Center for Rare Diseases of Thyroid and Hormone Receptivity, University Hospital of Angers , 49000 Angers , France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fr\u00e9d\u00e9ric","family":"Illouz","sequence":"additional","affiliation":[{"name":"Reference Center for Rare Diseases of Thyroid and Hormone Receptivity, University Hospital of Angers , 49000 Angers , France"},{"name":"Department of Endocrinology, Diabetes and Nutrition, University Hospital of Angers , 49000 Angers , France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica","family":"Amsellem Jager","sequence":"additional","affiliation":[{"name":"Department of Pediatric Endocrinology and Diabetology, University Hospital of Angers , 49000 Angers , France"},{"name":"Reference Center for Rare Diseases of Thyroid and Hormone Receptivity, University Hospital of Angers , 49000 Angers , France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anne","family":"Bachelot","sequence":"additional","affiliation":[{"name":"Department of Endocrinology and Reproductive Medicine, H\u00f4pital Piti\u00e9-Salp\u00eatri\u00e8re, ICAN , 75651 Paris , France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pascal","family":"Barat","sequence":"additional","affiliation":[{"name":"Pediatric Endocrinology, CHU 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