نتایج جستجو برای: thyroid dysgenesis

تعداد نتایج: 85068  

1997
Susan Ewart

Anterior segment dysgenesis syndrome is an inherited ocular defect in Rocky Mountain Horses. The disease is Mendelian with semidominant inheritance. Heterozygous animals have ciliary cysts, and homozygous animals have complex anterior segment dysgenesis. Authors’ address: Depts. of Large Animal Clinical Sciences (Ewart) and Small Animal Clinical Sciences (Ramsey), D202 Veterinary Medical Center...

Journal: :Archives of ophthalmology 2012
Nicholas J Butler Eric B Suhler

Comment. The first report of unilateral RPE dysgenesis was published in 2002. In this report, 3 young men and 1 woman aged 16 to 34 years were noted to have a round leopard-spot lesion contiguous with the optic nerve. In 2009, the typical characteristics of unilateral RPE dysgenesis were described in a set of 9 affected patients, 6 males and 3 females aged 14 to 42 years. The margin of the lesi...

Journal: :PLoS genetics 2016
Tom Hill Christian Schlötterer Andrea J Betancourt

In a classic example of the invasion of a species by a selfish genetic element, the P-element was horizontally transferred from a distantly related species into Drosophila melanogaster. Despite causing 'hybrid dysgenesis', a syndrome of abnormal phenotypes that include sterility, the P-element spread globally in the course of a few decades in D. melanogaster. Until recently, its sister species,...

Journal: :Journal of medical genetics 1970
J Chemke R Carmichael J M Stewart R H Geer A Robinson

Gonadal dysgenesis is a condition characterized by streak gonads in subjects who present the phenotypic appearance of females. In pure gonadal dysgenesis, unlike Turner's syndrome, no associated somatic anomalies are found; the adult is of normal or above average stature and may have eunuchoidal proportions (Sohval, 1965). The term 'XY gonadal dysgenesis' refers to patients with pure gonadal dy...

Journal: :American journal of medical genetics. Part A 2013
Shane C Quinonez John M Park Raja Rabah Kailey M Owens Beverly M Yashar Thomas W Glover Catherine E Keegan

Deletion of the distal segment of 9p causes a syndrome comprising trigonocephaly, minor anomalies, and intellectual disability. Patients with this condition also frequently present with genitourinary abnormalities including cryptorchidism, hypospadias, ambiguous genitalia, or 46,XY testicular dysgenesis. The region responsible for the gonadal dysgenesis has been localized to 9p24.3 with the lik...

Journal: :Journal of medical genetics 1977
W H Brooks J C Meek R N Schimke

Hashimoto's thyroiditis has previously been associated with gonadal dysgenesis. Recent evidence suggests that Graves's disease and Hashimoto's thyroiditis are disorders of cell-mediated immunity and may have a common genetic predisposition. However, patients with both Graves's disease and the Turner syndrome have been reported only rarely. Three such cases are presented and the relation among g...

2010
Christoph Dorn Uwe Ulrich

Disorders of sex development (DSD), previously referred to as intersex disorders, comprise a variety of congenital diseases with anomalies of the sex chromosome, the gonads, the reproductive ducts and the genitalia. DSD is loosely classified into four groups on the basis of histological features of the gonadal tissue: XX-DSD with two ovaries (female pseudohermaphroditism), XY-DSD with two testi...

2017
Casey M. Bergman Shunhua Han Michael G. Nelson Vladyslav Bondarenko Iryna Kozeretska

The Drosophila melanogaster P transposable element provides one of the best cases of horizontal transfer of a mobile DNA sequence in eukaryotes. Invasion of natural populations by the P element has led to a syndrome of phenotypes known as P-M hybrid dysgenesis that emerges when strains differing in their P element composition mate and produce offspring. Despite extensive research on many aspect...

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