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首页> 外文期刊>Journal of pediatric endocrinology & metabolism: JPEM >Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency
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Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency

机译:重组胰岛素样生长因子-1治疗对Majewski II型原发性侏儒症和肝功能不全患儿短期线性生长的影响

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We report the case of a boy affected by severe intrauterine and postnatal growth retardation, microcephaly, facial dysmorphisms and postnecrotic cirrhosis, diagnosed at birth as having Seckel syndrome, and subsequently confirmed as Majewski osteodysplastic primordial dwarfism type II (MOPD II) on the basis of clinical and radiological features of skeletal dysplasia. At our observation (6 years 7 months) he presented height - 10.3 standard deviation score (SDS), weight - 22.1 SDS, head circumference - 8 SDS, delayed bone age of 4 years with respect to chronological age. In consideration of the low levels of insulin-like growth factor-1 (IGF-1) as well as of hepatic insufficiency, we started the treatment with recombinant human IGF-1 (rhIGF-1) at the dose of 0.04 mg/kg in 2 doses/day, with an increase of 0.04 mg/kg after 1 week until the maximum dose of 0.12 mg/kg. We observed an early response to rhIGF-1 treatment, with a shift of height velocity from 1.8 cm/year ( - 4.6 SDS) at 4 cm/year ( - 1.9 SDS), and an increase in bone age of 1.5 years during the first 6 months. rhIGF-1 treatment does not seem to be able to replace the physiological action of IGF-1 in patients with MOPD II and hepatic insufficiency, however, it seems to preserve the typical growth pattern of MOPD II patients, avoiding a further widening of the growth deficiency in these subjects.
机译:我们报告了一例男孩,该男孩受到严重的子宫内和出生后生长迟缓,小头畸形,面部畸形和坏死后肝硬化的影响,在出生时被诊断为患有Seckel综合征,随后在以下基础上被确认为Majewski骨发育不良性原始侏儒症II型(MOPD II)骨骼发育异常的临床和放射学特征。在我们的观察(6年7个月)中,他呈现了身高-10.3标准偏差评分(SDS),体重-22.1 SDS,头围-8 SDS,相对于年龄年龄的4年延迟骨龄。考虑到胰岛素样生长因子-1(IGF-1)的水平低以及肝功能不全,我们开始以0.04 mg / kg的剂量使用重组人IGF-1(rhIGF-1)进行治疗。每天2剂,在1周后增加0.04 mg / kg,直到最大剂量为0.12 mg / kg。我们观察到对rhIGF-1治疗的早期反应,高度速度从1.8 cm /年(-4.6 SDS)移至4 cm /年(-1.9 SDS),并且在第一次使用中骨龄增加了1.5年6个月。 rhIGF-1治疗似乎不能代替MOPD II和肝功能不全的患者的IGF-1的生理作用,但是,它似乎保留了MOPD II患者的典型生长方式,避免了进一步扩大生长这些科目缺乏。

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