Early Therapeutic Intervention in a Child with Beckwith–Wiedemann Syndrome in Inpatient and Outpatient Conditions — Case Report

Teresa Kaczan, R. Śmigiel, Magdalena Kazimierska-Zając, R. Dymarek, J. Rosińćzuk
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Abstract

Introduction. The Beckwith–Wiedemann syndrome (BWS) is a rare disorder characterized by a wide spectrum of symptoms i.a. umbilical hernia or omphalocele, macroglossia and above-average pre/postnatal growth (macrosomia). Aim. To present a case report of a child with BWS who underwent an early logopedic intervention and rehabilitation procedures including Bobath neuro-developmental treatment (NDT) and orofacial stimulation based on the Castillo-Morales concept (CMC). Case Report. The paper presents a case of a girl with BWS and the course of her psychomotor development during the 24 months of her life. The child has numerous defects typical for this syndrome, i.e. facial dysmorphism, macrosomia, and significant hypertrophy of the tongue as well as embryonal carcinomas such as hepatoblastoma and neuroblastoma. Psychomotor development was assessed at the age of 12 months using the Munich Functional Developmental Diagnostics (MFDD). At the age of 2, development of fine and gross motor skills and independence level do not differ significantly from the norm. The biggest problem concerns verbalization of needs due to the enlarged tongue. The girl still remains under multidisciplinary team care and is intensively rehabilitated. Discussion. There is no doubt that the care of children with BWS requires an interdisciplinary team of specialists. The child needs not only proper physical development, but also correct interpersonal relationships built on verbal communication. Therapy should be started as early as possible before bad habits develop. Conclusions. The knowledge of clinical features characteristic for the syndrome allows for rapid diagnosis and providing interdisciplinary care since the moment of birth. Children with BWS develop in individual ways depending on the type of genetic cause and additional defects. The care of BWS children must involve permanent and interdisciplinary co-operation with many specialists. (JNNN 2019;8(1):23–29)
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贝克威氏综合征患儿住院和门诊的早期治疗干预-病例报告
介绍。贝克维斯-魏德曼综合征(BWS)是一种罕见的疾病,其特征是广泛的症状,如脐疝或脐膨出,大舌和高于平均水平的产前/产后生长(巨大儿)。的目标。提出一例BWS患儿的病例报告,该患儿接受了早期外科干预和康复治疗,包括基于Castillo-Morales概念(CMC)的Bobath神经发育治疗(NDT)和口面部刺激。病例报告。本文报告1例BWS女童及其24个月的精神运动发展历程。儿童有许多典型的这种综合征的缺陷,如面部畸形、巨大儿、明显的舌肥大以及胚胎癌,如肝母细胞瘤和神经母细胞瘤。在12个月大时使用慕尼黑功能发展诊断(MFDD)评估精神运动发展。在2岁时,精细和大肌肉运动技能的发展和独立水平与正常没有显著差异。最大的问题是由于舌头变大,需要用语言表达。这名女孩仍在多学科小组的护理下进行集中康复。讨论。毫无疑问,照顾患有BWS的儿童需要一个跨学科的专家团队。孩子不仅需要适当的身体发育,还需要建立在语言交流基础上的正确的人际关系。治疗应该在坏习惯形成之前尽早开始。结论。该综合征的临床特征的知识允许快速诊断和提供跨学科的护理,因为出生的那一刻。患有BWS的儿童有不同的发展方式,这取决于遗传原因和其他缺陷的类型。对残疾儿童的照料必须涉及与许多专家的长期和跨学科合作。(JNNN 2019; 8 (1): 23-29)
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