Ghosal hematodiaphyseal dysplasia

Ghosal hematodiaphyseal dysplasia
Thromboxane A2
Classification and external resources
OMIM 231095
DiseasesDB 34928

Ghosal hematodiaphyseal dysplasia is a metabolic disorder.

It is associated with diaphyseal dysplasia and refractory anemia.[1]

It is associated with a deficiency of Thromboxane-A synthase,[2] which produces Thromboxane A2.

It was characterized in 1988.[3]

References

  1. ↑ Isidor B, Dagoneau N, Huber C, et al. (April 2007). "A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34". Hum. Genet. 121 (2): 269–73. PMID 17203301. doi:10.1007/s00439-006-0311-1.
  2. ↑ Geneviève D, Proulle V, Isidor B, et al. (March 2008). "Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)". Nat. Genet. 40 (3): 284–6. PMID 18264100. doi:10.1038/ng.2007.66.
  3. ↑ Ghosal SP, Mukherjee AK, Mukherjee D, Ghosh AK (July 1988). "Diaphyseal dysplasia associated with anemia". J. Pediatr. 113 (1 Pt 1): 49–57. PMID 3385529. doi:10.1016/S0022-3476(88)80527-4.


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