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Naked foal syndrome (NFS) is a genetic disorder specific to the Akhal-Teke horse breed. A rare genodermatosis , it is characterized by almost complete hairlessness and mild ichthyosis . The condition is inherited as a monogenic autosomal recessive trait, and affected horses typically die between a few weeks and three years of age.
The Akhal-Teke, due to its natural athleticism, can be a sport horse, good at dressage, show jumping, eventing, racing, and endurance riding. A noted example was the Akhal-Teke stallion, Absent, who won the Grand Prix de Dressage at the 1960 Summer Olympics in Rome, while being ridden by Sergei Filatov.
Pages in category "Akhal-Teke horses" ... Naked foal syndrome; Y. Yanardag This page was last edited on 31 December 2018, at 19:02 ...
Nager acrofacial dysostosis, also known as Nager syndrome, is a genetic disorder which displays several or all of the following characteristics: underdevelopment of the cheek and jaw area, down-sloping of the opening of the eyes, lack or absence of the lower eyelashes, kidney or stomach reflux, hammer toes, shortened soft palate, lack of development of the internal and external ear, possible ...
It has stables for 600 horses. Along with the race track and stables, there are also 57 two-storied cottages and two family houses for 114 owners, kindergarten for 160 children, 2 markets, a playground and sports fields, as well as a social-cultural center.
Dyskeratosis congenita (DKC), also known as Zinsser-Engman-Cole syndrome, is a rare progressive congenital disorder with a highly variable phenotype. [3] The entity was classically defined by the triad of abnormal skin pigmentation, nail dystrophy, and leukoplakia of the oral mucosa, and myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML), but these components do not always occur. [3]
Yanardag is an Akhal-Teke horse bred by Geldy Kyarizov, [5] and foaled in Turkmenistan in 1991, [1] the year of Turkmenistan's independence from the Soviet Union. [1] Yanardag was named world champion of the breed in 1999 in Moscow, and was subsequently acquired by Saparmurat Niyazov, who was President of Turkmenistan 1990–2006.
Sanjad–Sakati syndrome (Middle East syndrome) is a rare autosomal recessive genetic condition seen in offspring of Middle Eastern origin. It was first described in Saudi Arabia, [ 1 ] but has been seen in Qatari, Kuwaiti, Omani and other children from the Middle East as well as elsewhere. [ 2 ]