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Results 1 - 10 of 52 for ring syndrome
  1. ... this disorder.Epilepsy is a common feature of ring chromosome syndromes, including ring chromosome 14. There may be something ... from a mother to her children. Ring 14 Ring 14 syndrome Ring chromosome 14 Genetic Testing Registry: Ring chromosome ...
  2. ... a parent to a child. R(20) syndrome Ring 20 syndrome Ring chromosome 20 Ring chromosome 20 epilepsy syndrome ...
  3. ... this disorder.Epilepsy is a common feature of ring chromosome syndromes, including ring chromosome 14. There may be something ... causes signs and symptoms similar to those of ring chromosome 14 syndrome (described above). Terminal deletion 14 syndrome is caused ...
  4. ... certain facial features. More About This Health Condition Ring chromosome 20 syndrome is caused by a chromosomal abnormality known as ... and its broken ends fuse together. People with ring chromosome 20 syndrome have one copy of this abnormal chromosome in ...
  5. ... a ring chromosome can also cause Wolf-Hirschhorn syndrome. Ring chromosomes occur when a chromosome breaks in two ... disorder is caused by chromosome 4 becoming a ring chromosome. In the remaining cases of Wolf-Hirschhorn syndrome, an affected individual inherits a copy of chromosome ...
  6. ... of 2q detected using FISH: Further support for "ring chromosome 2 syndrome". Am J Med Genet A. 2005 Feb 1; ... MG, Natacci F, Larizza L. Small familial supernumerary ring chromosome 2: FISH ... A. Myelodysplastic syndrome associated with trisomy 2. Clin Lab Haematol. 2005 ...
  7. ... chromosome 22 can also cause 22q13.3 deletion syndrome. A ring chromosome is a circular structure that occurs when ... is at chromosome position 22q13.3, people with ring chromosome 22 will ... of 22q13.3 deletion syndrome are probably related to the loss of multiple ...
  8. ... chromosome 22 can also cause 22q13.3 deletion syndrome. A ring chromosome is a circular structure that occurs when ... points is at position 22q13.3, people with ring chromosome 22 have similar ... of 22q13.3 deletion syndrome. They have determined that the loss of a ...
  9. ... Condition BBBG1 FXY GBBB1 midline 1 (Opitz/BBB syndrome) midline 1 ring finger midline-1 OGS1 OS OSX RNF59 TRI18_ ... M, Ropers HH, Ballabio A. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nat Genet. 1997 Nov; ...
  10. ... with certain dyes. These abnormal cells are called ring sideroblasts.In people with Pearson syndrome, the pancreas does not work as well as ...
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