The underlying cause of avascular necrosis (AVN) of the femoral head is often not apparent. We report the case of a 26 year old builder with a four month history of bilateral hip pain, and a diagnosis of bilateral femoral head avascular necrosis. Fabry's disease was identified as the probable cause. Since 2001, enzyme replacement therapy for Fabry's disease has become available, with a potential to influence the disease process, and this is of potential importance to clinicians treating AVN.
HayatK., AshfaqK., TagoI.A., BhattiA., MinhasS., MehboobG.Factors related development of traumatic osteonecrosis of the femoral head.The Journal of the Pakistan Orthopaedic Association2008; 20(2): 108–13.
SweeleyC.C., KlinoskyB.Fabry's disease: classification as a sphingolipidosis and partial characterisation of a novel glycolipid.J Biol Chem1963; 238: 3148–50.
6.
DesnickR.J., IoannouY.A., EngC.M.Alpha Galactosidase A deficiency: Fabry disease. In: ScriverC.R., BeaudetA.L., SlyW.S., ValleD., eds. The metabolic bases of inherited disease.8th ed.New York: McGraw-Hill, 2001; 3733–74.
7.
MeikleP.J., HopwoodJ.J., ClagueA.E., CareyW.F.Prevalence of lysosomal storage disorders.JAMA1999; 281: 249–54.
8.
LidoveO., BekriS., GoizetC.[Fabry disease: proposed guidelines from a French expert group for its diagnosis, treatment and follow-up].Presse Med2007; 36: 1084–97.
9.
ShelleyE.D., ShelleyW.B., KurczynskiT.W.Painful fingers, heat intolerance, and telangiectases of the ear: easily ignored childhood signs of Fabry disease.Pediatr Dermatol1995; 12: 215–9.
10.
MenkesD.L., O'NeilT.J., SaenzK.K.Fabry's disease presenting as syncope, angiokeratomas, and spoke-like cataracts in a young man: discussion of the differential diagnosis.Mil Med1997; 162: 773–6.
MayesJ.S., ScheererJ.B., SifersR.N., DonaldsonM.L.Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease.Clin Chim Acta1981; 112: 247–51.
16.
LienY.H., LaiL.W.Bilateral femoral and distal tibial osteonecrosis in a patient with Fabry disease.Am J Orthop2005; 34: 192–4.
17.
DesnickR.J., AllenK.Y., DesnickS.J., RamanM.K., BernlohrR.W., KrivitW.Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes.J Lab Clin Med1973; 81: 157–71.