Mucopolysaccharidosis type I in Morocco: clinical features and genetic profile

• Published in: Archives de pédiatrie : organe officiel de la Société française de pédiatrie Vol. 7; no. 6; pp. 597 - 604
• Main Authors: Alif, N, Hess, K, Straczek, J, Sebbar, S, Belahsen, Y, Mouane, N, Abkari, A, Nabet, P, Gelot, M A
• Format: Journal Article
• Language: French
• Published: France 01.06.2000
• Subjects: Adolescent; Adult; Child; Child, Preschool; Female; Genetic Counseling; Genetic Testing; Glycosaminoglycans - urine; Humans; Male; Morocco; Mucopolysaccharidosis I - genetics; Mucopolysaccharidosis I - pathology; Pedigree; Morocco
• ISSN: 0929-693X

Mucopolysaccharidoses (MPS) are inherited metabolic disorders due to lysosomal enzyme deficiencies, leading to glycosaminoglycan accumulation in lysosomes of different tissues. The aim of this study was to characterize MPS types, particularly MPS I, which are difficult to differentiate by clinical features. Over a period of three years (June 1996-May 1999), 16 Moroccan patients (3-20 years old) with MPS were investigated. Twelve of them came from the Souss region. In subjects with suspected clinical MPS I or II, the diagnosis was confirmed by biochemical investigations, which included the quantification of total glycosaminoglycans (GAGs) released in urine, their identification, and the assay of alpha-L-iduronidase activity in leucocytes. A molecular analysis was performed in parallel, to provide the genetic proof of the diagnosis. These 16 patients belonged to 12 families, nine of which were consanguineous (75%). Twelve patients had Hurler syndrome and three had Hurler/Scheie's syndrome; no case of Scheie's syndrome was observed. Short stature, coarse face, organomegaly, hernia, cardiac disease, mental delay and dysostosis were observed in variable degrees. We report three cases without corneal clouding. Increased total urinary GAGs, identified as dermatan sulfate and heparan sulfate by thin-layer chromatography and total deficiency of alpha-L-iduronidase activity, were noted in studied subjects. At the molecular level the P533R mutation was detected in 24 among 26 alleles studied. It is now possible to perform the screening of MPS I and II in Morocco by analysis of clinical, radiologic observations and biological investigation. The predominance of P533R mutation could permit the screening of healthy heterozygotes and genetic counselling for families of Moroccan descent.