Thyroid Dysgenesis

Known as: Dysgenesis, Thyroid, Thyroid Dysgenesis [Disease/Finding], Thyroid dysplasia 
Defective development of the THYROID GLAND. This concept includes thyroid agenesis (aplasia), hypoplasia, or an ectopic gland. Clinical signs usually… (More)
National Institutes of Health

Papers overview

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Review
2007
Review
2007
In many instances, the pathophysiology of thyroid dysgenesis (TD) remains as yet unclear and until relatively recently the… (More)
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2007
2007
Familial cases of congenital hypothyroidism from thyroid dysgenesis (TD) (OMIM 218700) occur with a frequency 15-fold higher than… (More)
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Highly Cited
2006
Highly Cited
2006
CONTEXT Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000-4000 at birth. In 80-85% of… (More)
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Highly Cited
2005
Highly Cited
2005
Thyroid dysgenesis (TD) is responsible for most cases of congenital hypothyroidism, a condition that affects about one in 4000… (More)
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Highly Cited
2002
Highly Cited
2002
Three genes, TTF1, TTF2, and PAX8, involved in thyroid gland development and migration have been identified. Yet systematic… (More)
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Highly Cited
2002
Highly Cited
2002
Thyroid dysgenesis is the most common cause of congenital hypothyroidism (CH) and its genetic basis is largely unknown. Here, we… (More)
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Highly Cited
2001
Highly Cited
2001
Although a few familial forms of congenital hypothyroidism (CH) due to thyroid dysgenesis (TD) have been reported, this disorder… (More)
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Highly Cited
2000
Highly Cited
2000
The homeobox gene Hex is expressed in the anterior visceral endoderm (AVE) and rostral definitive endoderm of early mouse embryos… (More)
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Highly Cited
1998
Highly Cited
1998
Permanent congenital hypothyroidism (CH) is a common disease that occurs in 1 of 3,000–4,000 newborns. Except in rare cases due… (More)
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Highly Cited
1998
Highly Cited
1998
Alteration of thyroid gland morphogenesis (thyroid dysgenesis) is a frequent human malformation. Among the one in three to four… (More)
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