Erschienen in:
01.04.2011 | Original Article
Growth, final height and endocrine sequelae in a UK population of patients with Hurler syndrome (MPS1H)
verfasst von:
Chris J. Gardner, Nicola Robinson, Tim Meadows, Robert Wynn, Andrew Will, Jean Mercer, Heather J. Church, Karen Tylee, J. Edmond Wraith, Peter E. Clayton
Erschienen in:
Journal of Inherited Metabolic Disease
|
Ausgabe 2/2011
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Abstract
Objective
Hurler Syndrome, (MPSIH) is an inborn error of glycosaminoglycan metabolism. Haematopoietic stem cell transplantation (HSCT) has transformed the prognosis for these children. Prior to transplant patients receive chemotherapy or chemo-radiotherapy. Regular screening for the development of endocrine sequelae is therefore essential. We present for the first time data on final adult height and endocrine complications in children with MPSIH post HSCT.
Design
Retrospective case note study and a prospective programme of growth and endocrine assessment.
Patients
22 patients were included, mean age at last assessment 12.2 (Range 6.3–21.6) years. Mean age at HSCT was 1.3 (SD 0.6) years. Conditioning included mostly busulphan and cyclophosphamide, with 5 patients receiving total body irradiation prior to second transplant.
Results
Height SDS decreased over time. Final height (FH) was attained in seven patients with male FH SDS −4.3 (Range −3.8, −5.1) and female FH SDS −3.4 (Range −2.9, −5.6). Eight of 13 patients tested had evidence of high growth hormone (GH) levels, while one had GH deficiency. Adrenal and thyroid function was normal in all. 11 patients were pubertal or post pubertal. Two females had pubertal failure requiring intervention. All male patients had spontaneous, complete puberty; however three patients have reduced testicular volumes. Five out of 13 patients tested had an abnormal oral glucose tolerance test.
Conclusion
Growth is impaired, primarily related to skeletal dysplasia, but also associated with GH resistance. Pubertal development may be compromised and abnormalities of glucose metabolism are common. We recommend a structured endocrine surveillance programme for these patients.