Christodoulou Loucas, Krishnaiah Anil, Spyridou Christina, Salpietro Vincenzo, Hannan Siobhan, Saggar Anand, Mankad Kshitij, Deep Akash, Kinali Maria
1 Department of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London, UK ; 2 BUPA Cromwell Hospital, London, UK ; 3 St Mary's Hospital, Imperial College NHS trust, London, UK ; 4 St George's Hospital, NHS Foundation Trust, London, UK ; 5 Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK ; 6 King's College Hospital, NHS Foundation Trust, London, UK.
Quant Imaging Med Surg. 2015 Jun;5(3):476-9. doi: 10.3978/j.issn.2223-4292.2014.11.18.
Kenny Caffey syndrome (KCS) is a rare syndrome reported almost exclusively in Middle Eastern populations. It is characterized by severe growth retardation-short stature, dysmorphic features, episodic hypocalcaemia, hypoparathyroidism, seizures, and medullary stenosis of long bones with thickened cortices. We report a 10-year-old boy with KCS with an unusually severe respiratory and gastrointestinal system involvement-features not previously described in the literature. He had severe psychomotor retardation and regressed developmentally from walking unaided to sitting with support. MRI brain showed bilateral hippocampal sclerosis, marked supra-tentorial volume loss and numerous calcifications. A 12 bp deletion of exon 2 of tubulin-specific chaperone E (TBCE) gene was identified and the diagnosis of KCS was confirmed. Hypercarbia following a sleep study warranted nocturnal continuous positive airway pressure (CPAP) when aged 6. When boy aged 8, persistent hypercarbia with increasing oxygen requirement and increased frequency and severity of lower respiratory tract infections led to progressive respiratory failure. He became fully dependent on non-invasive ventilation and by 9 years he had a tracheotomy and was established on long-term ventilation. He developed retching, vomiting and diarrhea. Chest CT showed changes consistent with chronic aspiration, but no interstitial pulmonary fibrosis. He died aged 10 from respiratory complications.
肯尼·卡菲综合征(KCS)是一种罕见综合征,几乎仅在中东人群中报道。其特征为严重生长发育迟缓——身材矮小、畸形特征、发作性低钙血症、甲状旁腺功能减退、癫痫发作以及长骨骨髓狭窄伴皮质增厚。我们报告一名患有KCS的10岁男孩,其呼吸系统和胃肠道系统受累异常严重,这些特征此前文献中未曾描述。他有严重的精神运动发育迟缓,发育从独立行走退步到需支撑才能坐立。脑部磁共振成像(MRI)显示双侧海马硬化、幕上显著体积缩小以及大量钙化。鉴定出微管蛋白特异性伴侣E(TBCE)基因外显子2有12个碱基对缺失,从而确诊为KCS。6岁时睡眠研究后出现高碳酸血症,因此需要夜间持续气道正压通气(CPAP)。男孩8岁时,持续高碳酸血症伴氧需求增加以及下呼吸道感染频率和严重程度增加,导致进行性呼吸衰竭。他完全依赖无创通气,到9岁时进行了气管切开术并开始长期通气。他出现干呕、呕吐和腹泻。胸部CT显示与慢性误吸相符的改变,但无间质性肺纤维化。他10岁时死于呼吸并发症。