Lingappa Lokesh, Shah Nikit, Motepalli Ananth Sagar, Shaik Farhan
Department of Pediatric Neurology, Rainbow Children's Hospital, Banjara Hills, Hyderabad, Telangana, India.
Department of Pediatric Critical Care, Rainbow Children's Hospital, Banjara Hills, Hyderabad, Telangana, India.
Ann Indian Acad Neurol. 2016 Jul-Sep;19(3):395-8. doi: 10.4103/0972-2327.168635.
Spinal muscular atrophy with respiratory distress syndrome (SMARD1) is a rare cause of early infantile respiratory failure and death. No cases have been currently described from India. Two low-birth-weight infants presented prior to 6 months of age with recurrent apnea and respiratory distress. Both required prolonged ventilation, and had distal arthrogryposis and diaphragmatic eventration. Nerve conduction study revealed motor sensory axonopathy. Genetic testing confirmed mutations in immunoglobulin mu binding protein (IGHMBP2). These two cases establish presence of SMARD1 in our population. Both infants died on discontinuation of ventilation. Antenatal diagnoses done in one pregnancy. Though rare, high index of suspicion is essential in view of poor outcome and aid antenatal counseling.
伴有呼吸窘迫综合征的脊髓性肌萎缩症(SMARD1)是早期婴儿呼吸衰竭和死亡的罕见原因。目前印度尚无相关病例报道。两名低体重儿在6个月龄前出现反复呼吸暂停和呼吸窘迫。两人均需要长期通气,且有远端关节挛缩和膈膨出。神经传导研究显示运动感觉轴索性神经病。基因检测证实免疫球蛋白μ结合蛋白(IGHMBP2)存在突变。这两例病例证实了我国人群中存在SMARD1。两名婴儿在通气中断后均死亡。其中一次妊娠进行了产前诊断。尽管罕见,但鉴于预后不良,高度怀疑至关重要,有助于产前咨询。