Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series

被引:6
作者
Kilavuz, Sebile [1 ]
Basaran, Sibel [2 ]
Kor, Deniz [1 ]
Bulut, Fatma Derya [1 ]
Erdem, Sevcan [3 ]
Balli, Huseyin Tugsan [4 ]
Dagkiran, Muhammed [5 ]
Bisgin, Atil [6 ]
Mungan, Halise Neslihan Onenli [7 ]
机构
[1] Cukurova Univ, Div Pediat Metab & Nutr, Dept Pediat, Fac Med, Adana, Turkey
[2] Cukurova Univ, Dept Phys Med & Rehabil, Fac Med, Adana, Turkey
[3] Cukurova Univ, Div Pediat Cardiol, Dept Pediat, Fac Med, Adana, Turkey
[4] Cukurova Univ, Dept Radiol, Fac Med, Adana, Turkey
[5] Cukurova Univ, Dept Ear Nose & Throat Dis, Fac Med, Adana, Turkey
[6] Cukurova Univ, Dept Med Genet, Fac Med, AGENTEM Adana Genet Dis Diag & Treatment Ctr, Adana, Turkey
[7] Cukurova Univ, Div Pediat Metab & Nutr, Dept Pediat, Fac Med, TR-01130 Adana, Turkey
关键词
Elosulfase alfa; Enzyme replacement therapy; Mucopolysaccharidosis IVA; Morquio A syndrome;
D O I
10.1186/s13023-021-01761-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background This case series includes longitudinal clinical data of ten patients with Morquio A syndrome from south and southeastern parts of Turkey, which were retrospectively collected from medical records. All patients received enzyme replacement therapy (ERT). Clinical data collected included physical appearance, anthropometric data, neurological and psychological examinations, cardiovascular evaluation, pulmonary function tests, eye and ear-nose-throat examinations, endurance in the 6-min walk test and/or 3-min stair climb test, joint range of motion, and skeletal investigations (X-rays, bone mineral density). Results At the time of ERT initiation, two patients were infants (1.8 and 2.1 years), five were children (3.4-7.1 years), and three were adults (16.5-39.5 years). Patients had up to 4 years follow-up. Most patients had classical Morquio A, based on genotypic and phenotypic data. Endurance was considerably reduced in all patients, but remained relatively stable or increased over time in most cases after treatment initiation. Length/height fell below normal growth curves, except in the two infants who started ERT at <= 2.1 years of age. All patients had skeletal and/or joint abnormalities when ERT was started. Follow-up data did not suggest improvements in skeletal abnormalities, except in one of the younger infants. Nine patients had corneal clouding, which resolved after treatment initiation in the two infants, but not in the other patients. Hepatomegaly was reported in seven patients and resolved with treatment in five of them. Other frequent findings at treatment initiation were coarse facial features (N = 9), hearing loss (N = 6), and cardiac abnormalities (N = 6). Cardiac disease deteriorated over time in three patients, but did not progress in the others. Conclusions Overall, this case series with Morquio A patients confirms clinical trial data showing long-term stabilization of endurance after treatment initiation across ages and suggest that very early initiation of ERT optimizes growth outcomes.
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页数:10
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