- Two Cases of Xp21 Contiguous Gene Deletion Syndrome
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Ye GY, Choi HS, Park JM, Lee HJ, Kim WM
- KMID: 2324528
- J Korean Acad Rehabil Med.
- 2007 Apr;31(2):243-247.
On chromosome Xp21 region, several genes such as glycerol kinase (GK) gene, adrenal hypoplasia congenita gene and Duchenne muscular dystrophy gene are located contiguously. Xp21 contiguous gene deletion syndrome involves... -
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- A Case of Xp21 Contiguous Gene Deletion Syndrome with Hyperglycerolemia, Congenital Adrenal Hypoplasia and Duchenne Muscular Dystrophy
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Shin DW, Huh J, Lee HJ, Park WI, Lee KJ, Shin YS, Sjarif DR, Poll-The B
- KMID: 1605945
- J Korean Pediatr Soc.
- 2001 Jan;44(1):83-88.
On Xp21 region several genes such as adrenal hypoplasia congenita(AHC) gene, glycerol kinase (GK) gene and Duchenne muscular dystrophy(DMD) gene are located contiguously. If there is a long deletion in... -
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- Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome
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Koh JW, Kang SY, Kim GH, Yoo HW, Yu J
- KMID: 2047468
- Ann Pediatr Endocrinol Metab.
- 2013 Jun;18(2):90-94.
- doi: 10.6065/apem.2013.18.2.90
X-linked adrenal hypoplasia congenita is caused by the mutation of DAX-1 gene (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1), and can occur as part of... -
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- Application of New Pathogenesis on the Drug Treatment of Diabetes
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Kim YS
- KMID: 2183144
- J Korean Med Assoc.
- 2003 Dec;46(12):1128-1140.
- doi: 10.5124/jkma.2003.46.12.1128
Patients with type 2 diabetes mellitus are associated with insulin resistance and/or impaired insulin secretion. Previous observations indicate that patients with type 2 diabetes tend to have an impaired insulin... -
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