Search results
Results From The WOW.Com Content Network
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 has a refined head with predominantly a straight or slightly convex profile, and long ears. It can also have almond-shaped or "hooded" eyes. [45] The mane and tail are usually sparse. The long back is lightly muscled, and is coupled to a flat croup and long, upright neck. The Akhal-Teke possess sloping shoulders and thin skin.
Jeune syndrome is a rare genetic disorder that affects the way a child's cartilage and bones develop. It begins before the child is born and primarily affects the child's rib cage, pelvis, arms and legs. [5] Usually, problems with the rib cage cause the most serious health problems for children with Jeune syndrome.
The Turkoman horse, or Turkmene, is an Oriental horse breed from the steppes of Central Asia.It influenced many modern horse breeds, including the Thoroughbred horse. Modern descendants include the Akhal-Teke, [1] the Iomud, the Goklan and Nokhorli. [2]
MICPCH in males may occur with or without severe epileptic encephalopathy (Ohtahara syndrome, West syndrome, or early myoclonic epilepsy) in addition to severe-to-profound developmental delay. When seizures are present, they occur early and may be intractable. [7] Prognosis is poor for males with this condition. [8]
Okamoto syndrome was first described in 1997 by Nobuhiko Okamoto et al. from the Department of Medical Genetics at Osaka Women's and Children's Hospital after observing very similar symptoms and physical features in two unrelated Japanese infants. Both infants had congenital hydronephrosis due to ureteropelvic junction stenosis, low muscle tone ...
The US and UK don't even remotely rank close to the top spots.
Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy. These calcium deposits decrease the size of cranial foramina, and can decrease the circumference of the cervical spinal canal ...