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Macroorchidism

Known as: Large testicles, Large testis 
The presence of abnormally large testes. [HPO:probinson]
National Institutes of Health

Related topics

Related topics

5 relations
AspartylglucosaminuriaAtkin syndromeClark-Baraitser syndromeFragile X Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Identification of an IGSF1‐specific deletion in a five‐generation pedigree with X‐linked Central Hypothyroidism without macroorchidism
IGSF1 deficiency syndrome (IDS) is a recently described X‐linked congenital central hypothyroidism disorder characterized by loss… 
2013
2013
A novel mutation of IGSF1 in a Japanese patient of congenital central hypothyroidism without macroorchidism.
Congenital central hypothyroidism (C-CH) is a rare disease known to be caused by mutations of the genes encoding TSH β or the TRH… 
Highly Cited
1996
Highly Cited
1996
A simplified six-item checklist for screening for fragile X syndrome in the pediatric population.
1991
1991
Macroorchidism and testicular fibrosis associated with autoimmune thyroiditis
A 16-year-old male with long-standing atrophic chronic lymphocytic thyroiditis was evaluated for macroorchidism. A testicular… 
1988
1988
Ethnic differences in testis size: a possible link with the cytogenetics of true hermaphroditism.
Data on human testis size, although scanty and suffering from lack of standardization, suggest the existence of marked ethnic… 
Highly Cited
1988
Highly Cited
1988
Hypothalamic-pituitary gonadal axis in boys with primary hypothyroidism and macroorchidism.
Review
1984
Review
1984
"De Novo" trisomy 20p with macroorchidism in a prepuberal boy.
A 9-year-old prepuberal boy with trisomy 20p syndrome and previously undescribed macroorchidism is presented. This is the second… 
Highly Cited
1984
Highly Cited
1984
An anthropometric study of males with the fragile-X syndrome.
Anthropometric methods were used to examine 18 males 18 to 69 years old with the Fragile-X syndrome. Thirteen of 15 subjects had… 
Review
1983
Review
1983
The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers.
An epidemiological study was carried out on the group of moderately retarded brothers (IQ, 30-55) identified by Turner and Turner… 
Highly Cited
1982
Highly Cited
1982
Marker X syndrome in an oriental family with probable transmission by a normal male.
We report an oriental family with sex-linked mental retardation, macroorchidism, and a marker or fragile site on the X chromosome… 
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