arthrogryposis sentence in Hindi
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- The underlying aetiology and pathogenesis of congenital contractures, particularly arthrogryposis and the mechanism of the mutations remains an active area of investigation.
- In March 2006, Stevenson et al . published strict diagnostic criteria for distal arthrogryposis type 2A ( DA2A ) or Freeman Sheldon syndrome.
- Mutations in this gene have been associated with two congenital contracture ( arthrogryposis ) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome.
- These included two or more features of distal arthrogryposis : microstomia, whistling-face, nasolabial creases, and'H-shaped'chin dimple.
- Martina's particular type of arthrogryposis _ meaning " stiff joints " _ occurs in one out of perhaps 50, 000 births, says Burke.
- Joshua suffers from a birth defect affecting the bones called arthrogryposis, Menard said, adding that the braces were paid for only after a protracted fight with Medicaid officials.
- Services are provided for people with physical conditions ranging from the very rare to the more familiar, such as cerebral palsy, spina bifida, muscular dystrophy and arthrogryposis.
- Mutations in the related but distinct genes encoding the slow-type and cardiac-type isoforms have been associated with distal arthrogryposis, type 1 and hypertrophic cardiomyopathy, respectively.
- Overton has arthrogryposis multiplex congenita, a medical condition which " causes muscle weakness and a tendency for bones to break easily . " It also results in joints that are immobile.
- Born with arthrogryposis, a rare occurrence where missing muscle mass and bone deformities limit range of motion, Samantha wasn't able to bring a spoon to her mouth without spilling.
- Dr . Stephen Burke, a pediatric orthopedic surgeon at the Hospital for Special Surgery, also took his team to Italy last month, examining about 30 children with symptoms of arthrogryposis.
- Dundar et al . described patients with Mental Motor Retardation, ocular abnormality, dysmorphic facial appearance, long fingers, and distal arthrogryposis with severely adducted thumbs and clubfeet in Turkish family in 1997.
- The malformations of arthrogryposis can be secondary to environmental factors such as : decreased intrauterine movement, oligohydramnios ( low volume or abnormal distribution of intrauterine fluid ), and defects in the fetal blood supply.
- Other mutations that could cause arthrogryposis are : single gene defects ( X-linked recessive, autosomal recessive and autosomal dominant ), mitochondrial defects and chromosomal disorders ( for example : trisomy 18 ).
- Competitors with multiple sclerosis, muscular dystrophy and arthrogryposis were not eligible for classification by CP-ISRA, but were eligible for classification by International Sports Organisation for the Disabled for the Games of Les Autres.
- The disorder, called arthrogryposis multiplex congenital, is typically the result of a fetus that has too little room to move in the uterus, causing protective tissue to grow around the joints and fixing them in position.
- It is no longer a common operation, but is still used in cases of a deformed calcaneus, foot paralysis following poliomyelitis, and rigid clubfoot deformities that are secondary to spina bifida or arthrogryposis ( AMC ).
- A missense mutation R174Q, a nonsense mutation R156X, and three single residue deletions DE167, DK175 and DK176, all in the C-terminal actin-tropomyosin interacting domain, have been found in patients with distal arthrogryposis.
- When they are poisoned by " C . maculatum " during the fetus'organ formation period, the offspring is born with malformations, mainly palatoschisis and multiple congenital contractures ( MCC; frequently described as arthrogryposis ).
- Martina's particular type of arthrogryposis _ meaning " stiff joints " _ occurs in one out of perhaps 50, 000 births, said Dr . Stephen Burke, a pediatric orthopedic surgeon at the Hospital for Special Surgery.
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