Pacman dysplasia
From Wikipedia, the free encyclopedia
Pacman dysplasia is a lethal autosomal recessive skeletal dysplasia
[edit] References
- Wilcox WR, Wenger DA, Lachman RS, Rimoin DL (2005). "Distinguishing Pacman dysplasia from mucolipidosis II: comment on Saul et al. [2005]". Am J Med Genet A 135 (3): 333. doi: . PMID 15887286.
- Saul RA, Proud V, Taylor HA, Leroy JG, Spranger J (2005). "Prenatal mucolipidosis type II (I-cell disease) can present as Pacman dysplasia". Am J Med Genet A 135 (3): 328–32. doi: . PMID 15887289.
- Wilcox WR, Lucas BC, Loebel B, Bachman RP, Lachman RS, Rimoin DL (1998). "Pacman dysplasia: report of two affected sibs". Am J Med Genet 77 (4): 272–6. doi: . PMID 9600734.
- Shohat M, Rimoin DL, Gruber HE, Lachman R (1993). "New epiphyseal stippling syndrome with osteoclastic hyperplasia". Am J Med Genet 45 (5): 558–61. doi: . PMID 8456823.
- Miller SF, Proud VK, Werner AL, Field FM, Wilcox WF, Lachman RS, Rimoin DL (2003). "Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic features". Pediatr Radiol 33 (4): 256–60. doi: . PMID 12709756.