The Journal of Pediatrics
Volume 156, Issue 5 , Pages 828-831, May 2010

Misdiagnosis in Fabry Disease

This work was presented in part at the 60th annual meeting of the American Academy of Neurology, Chicago, IL, April, 2008. The authors declare no conflicts of interest.

  • Cintia L. Marchesoni, MD

      Affiliations

    • Neurology Department, Hospital Británico de Buenos Aires, Buenos Aires, Argentina
  • ,
  • Norma Roa

      Affiliations

    • Hematology Service, Instituto Médico Quilmes, Quilmes, Argentina
  • ,
  • Ana María Pardal, MD

      Affiliations

    • Neurology Department, Hospital Británico de Buenos Aires, Buenos Aires, Argentina
  • ,
  • Pablo Neumann, MD

      Affiliations

    • Nephrology Department, Hospital Italiano, La Plata, Argentina
  • ,
  • Guillermo Cáceres, MD

      Affiliations

    • Biochemistry Laboratory, Hospital Interzonal Pinamar, Pinamar, Argentina
  • ,
  • Pablo Martínez, Bioch

      Affiliations

    • Pediatric Service, Hospital Interzonal de Bahía Blanca, Bahía Blanca, Argentina
  • ,
  • Isaac Kisinovsky, MD

      Affiliations

    • Hematology Service, Instituto Médico Quilmes, Quilmes, Argentina
  • ,
  • Silvia Bianchi, MD

      Affiliations

    • Pediatric Service, Centro Fabry de Tucumán, Tucumán, Argentina
  • ,
  • Ana Lía Tarabuso, MD

      Affiliations

    • Dermatology Service, CEAL Centro Médico, Chubut, Trelew, Argentina
  • ,
  • Ricardo C. Reisin, MD

      Affiliations

    • Neurology Department, Hospital Británico de Buenos Aires, Buenos Aires, Argentina
    • Corresponding Author InformationReprint requests: Ricardo C. Reisin, Neurology Department, Hospital Británico, Perdriel 74, Buenos Aires 1280, Argentina.

Received 19 April 2009; received in revised form 2 December 2009; accepted 8 February 2010.

Objective

To evaluate the most frequent diagnostic errors in patients with Fabry disease and the types of specialists most often consulted before diagnosis.

Study design

We evaluated 45 consecutive symptomatic patients with Fabry disease confirmed by enzymatic tests in males and genetic studies in females. We interviewed the patients, their mothers, or both regarding symptoms, age at onset, medical consultations, and recommended treatments.

Results

Neuropathic pain was the most frequent initial complaint, and rheumatic fever was the most common diagnosis. Seven patients were treated with penicillin for many years. Ten patients sought medical consultation because of abdominal pain and were diagnosed with food intoxication or nonspecific pain. Six patients sought consultation because of anhidrosis, considered of unclear cause, and angiokeratomas diagnosed as petechiae. Internists and pediatricians were the most frequently consulted specialists. The correct diagnosis was obtained after a mean of 19.7 years.

Conclusions

Pediatricians as well as internists commonly misdiagnose Fabry disease. Neuropathic pain, hypohidrosis, and recurrent abdominal pain in childhood or adolescence should include Fabry disease in the differential diagnosis to facilitate earlier diagnosis and treatment of these patients.

AADELFA, Asociación Argentina de Enfermedad de Fabry y Otras Enfermedades Lisosomales, ERT, Enzyme replacement therapy

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PII: S0022-3476(10)00136-8

doi:10.1016/j.jpeds.2010.02.012

Refers to article:

  • Four-Year Prospective Clinical Trial of Agalsidase Alfa in Children with Fabry Disease , 25 January 2010

    Raphael Schiffmann, Rick A. Martin, Tyler Reimschisel, Karen Johnson, Victoria Castaneda, Y. Howard Lien, Gregory M. Pastores, Christoph Kampmann, Markus Ries, Joe T.R. Clarke
    The Journal of Pediatrics May 2010 (Vol. 156, Issue 5, Pages 832-837.e1)

The Journal of Pediatrics
Volume 156, Issue 5 , Pages 828-831, May 2010