相似文献
1
Mucopolysaccharidosis type IV (Morquio syndrome).
J Assoc Physicians India. 2007 Jun;55:434.
2
Unclassified short stature, possibly spondyloepiphyseal dysplasia, possibly multiple epiphyseal dysplasia, in father and daughter.
Birth Defects Orig Artic Ser. 1974;10(12):399-405.
3
Pleomorphism of hip disease in a large kinship with spondylo- and multiple epiphyseal dysplasia.
Birth Defects Orig Artic Ser. 1974;10(12):406-11.
4
Morquio syndrome: clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVB.
Hum Genet. 1981;57(4):360-5. doi: 10.1007/BF00281685.
5
Hip arthrography in the epiphyseal dysplasias.
Birth Defects Orig Artic Ser. 1974;10(12):186-95.
6
[Congenital spondylo-epiphyseal dysplasia].
Kinderarztl Prax. 1969 Apr;37(4):161-6.
7
Progressive mental regression in siblings with Morquio disease type B (mucopolysaccharidosis IV B).
Clin Genet. 1987 Nov;32(5):313-25. doi: 10.1111/j.1399-0004.1987.tb03296.x.
8
Two brothers with nonkeratan-sulfate-excreting Morquio syndrome.
Birth Defects Orig Artic Ser. 1974;10(12):466-9.
9
The Kniest syndrome.
Birth Defects Orig Artic Ser. 1974;10(9):193-208.
10
[Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio disease].
Arch Pediatr. 2001 Aug;8(8):838-42. doi: 10.1016/s0929-693x(01)00544-9.
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