Monozygotic Twins Discordant for ROHHAD Phenotype

被引:40
|
作者
Patwari, Pallavi P. [1 ]
Rand, Casey M. [1 ]
Berry-Kravis, Elizabeth M. [2 ,3 ,4 ]
Ize-Ludlow, Diego [5 ]
Weese-Mayer, Debra E. [1 ]
机构
[1] Northwestern Univ, Childrens Mem Hosp, Feinberg Sch Med, Ctr Auton Med Pediat,Dept Pediat, Chicago, IL 60614 USA
[2] Rush Univ, Med Ctr, Dept Pediat, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[4] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL 60612 USA
[5] Univ Illinois, Dept Pediat, Div Endocrinol, Chicago, IL USA
关键词
autonomic nervous system; late-onset central hypoventilation syndrome; tumors of neural crest origin; overweight children; diabetes insipidus; IDIOPATHIC HYPOTHALAMIC DYSFUNCTION; RAPID-ONSET OBESITY; HYPOVENTILATION SYNDROME; AUTONOMIC DYSREGULATION; PARANEOPLASTIC-SYNDROME; MANIFESTATIONS; CHILDHOOD;
D O I
10.1542/peds.2011-0155
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD) falls within a group of pediatric disorders with both respiratory control and autonomic nervous system dysregulation. Children with ROHHAD typically present after 1.5 years of age with rapid weight gain as the initial sign. Subsequently, they develop alveolar hypoventilation, autonomic nervous system dysregulation, and, if untreated, cardiorespiratory arrest. To our knowledge, this is the first report of discordant presentation of ROHHAD in monozygotic twins. Twin girls, born at term, had concordant growth and development until 8 years of age. From 8 to 12 years of age, the affected twin developed features characteristic of ROHHAD including obesity, alveolar hypoventilation, scoliosis, hypothalamic dysfunction (central diabetes insipidus, hypothyroidism, premature pubarche, and growth hormone deficiency), right paraspinal/thoracic ganglioneuroblastoma, seizures, and autonomic dysregulation including altered pain perception, large and sluggishly reactive pupils, hypothermia, and profound bradycardia that required a cardiac pacemaker. Results of genetic testing for PHOX2B (congenital central hypoventilation syndrome disease-defining gene) mutations were negative. With early recognition and conservative management, the affected twin had excellent neurocognitive outcome that matched that of the unaffected twin. The unaffected twin demonstrated rapid weight gain later in age but not development of signs/symptoms consistent with ROHHAD. This discordant twin pair demonstrates key features of ROHHAD including the importance of early recognition (especially hypoventilation), complexity of signs/symptoms and clinical course, and importance of initiating comprehensive, multispecialty care. These cases confound the hypothesis of a monogenic etiology for ROHHAD and indicate alternative etiologies including autoimmune or epigenetic phenomenon or a combination of genetic predisposition and acquired precipitant. Pediatrics 2011; 128: e711-e715
引用
收藏
页码:E711 / E715
页数:5
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