Endocrine manifestations of the rapid-onset obesity with hypoventilation, hypothalamic, autonomic dysregulation, and neural tumor syndrome in childhood

被引:85
作者
Bougneres, Pierre [1 ]
Pantalone, Letitia [1 ]
Linglart, Agnes [1 ]
Rothenbuehler, Anya [1 ]
Le Stunff, Catherine [1 ]
机构
[1] Hop St Vincent de Paul, Dept Pediat Endocrinol, F-75014 Paris, France
关键词
D O I
10.1210/jc.2008-0238
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Context: Rapid-onset obesity with hypoventilation, hypothalamic, autonomic dysregulation, and neural tumor (ROHHADNET) is a newly described syndrome that can cause cardiorespiratory arrests and death. It mimics several endocrine disorders or genetic obesity syndromes during early childhood and is associated with various forms of hypothalamic-pituitary endocrine dysfunctions that have not yet been fully investigated. Objective: The current report aspires to facilitate the earlier recognition and appropriate treatment of the ROHHADNET syndrome when children present with various endocrine manifestations, such as early obesity, growth failure, pseudo-Cushing's syndrome, glucocorticoid insufficiency, congenital hypopituitarism, or adrenal tumors. A more widespread knowledge of the syndrome will help characterize its molecular origin. Design: Endocrine studies were performed in six patients admitted for seemingly common early-onset obesity associated with growth failure in five of them. The six patients later showed distinctive features of the ROHHADNET syndrome. Results: Abnormalities of the pituitary adrenal axis ranged from a true Cushing-like profile (one of six), to glucocorticoid deficiency with normal ACTH (two of six). Complete GH deficiency with low IGF-I was observed in four of six, hypogonadotropic hypogonadism in four of six, hyperprolactinemia in six of six, and various degrees of TSH/T-4 abnormalities in five of five patients. All had increased natremia without diabetes insipidus. Five children had unilateral macroscopic adrenal ganglioneuroma. Two patients died at 8.5 and 12 yr of age. Conclusions: Various hypothalamic-pituitary endocrine dysfunctions are associated with ROHHADNET, carrying a risk of misdiagnosis until other elements of the syndrome make it more easily recognizable. Given its severity, ROHHADNET syndrome should be considered in all cases of isolated, rapid, and early obesity.
引用
收藏
页码:3971 / 3980
页数:10
相关论文
共 69 条
[1]
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome [J].
Amiel, J ;
Laudier, B ;
Attié-Bitach, T ;
Trang, H ;
de Pontual, L ;
Gener, B ;
Trochet, D ;
Etchevers, H ;
Ray, P ;
Simonneau, M ;
Vekemans, M ;
Munnich, A ;
Gaultier, C ;
Lyonnet, S .
NATURE GENETICS, 2003, 33 (04) :459-461
[2]
Development of novel tools for the diagnosis and prognosis of pheochromocytoma using peptide marker immunoassay and gene expression profiling approaches [J].
Anouar, Youssef ;
Yon, Laurent ;
Guillemot, Johann ;
Thouennon, Erwan ;
Barbier, Laure ;
Gimenez-Roqueplo, Anne-Paule ;
Bertherat, Jerome ;
Lefebvre, Herve ;
Klein, Marc ;
Muresan, Mihaela ;
Grouzmann, Eric ;
Plouin, Pierre-Francois ;
Vaudry, Hubert ;
Elkahloun, Abdel G. .
PHEOCHROMOCYTOMA, 2006, 1073 :533-540
[3]
Diagnosis and complications of Cushing's syndrome: A consensus statement [J].
Arnaldi, G ;
Angeli, A ;
Atkinson, AB ;
Bertagna, X ;
Cavagnini, F ;
Chrousos, GP ;
Fava, GA ;
Findling, JW ;
Gaillard, RC ;
Grossman, AB ;
Kola, B ;
Lacroix, A ;
Mancini, T ;
Mantero, F ;
Newell-Price, J ;
Nieman, LK ;
Sonino, N ;
Vance, ML ;
Giustina, A ;
Boscaro, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (12) :5593-5602
[4]
Corticotroph tumor progression after adrenalectomy in Cushing's disease:: A reappraisal of Nelson's syndrome [J].
Assie, Guillaume ;
Bahurel, Helene ;
Coste, Joel ;
Silvera, Stephane ;
Kujas, Michele ;
Dugue, Marie-Annick ;
Karray, Foued ;
Dousset, Bertrand ;
Bertherat, Jerome ;
Legmann, Paul ;
Bertagna, Xavier .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (01) :172-179
[5]
Detection of adrenocorticotropin-secreting pituitary adenomas by magnetic resonance imaging in children and adolescents with Cushing disease [J].
Batista, D ;
Courkoutsakis, NA ;
Oldfield, EH ;
Griffin, KJ ;
Keil, M ;
Patronas, NJ ;
Stratakis, CA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (09) :5134-5140
[6]
Diagnostic tests for children who are referred for the investigation of Cushing syndrome [J].
Batista, Dalia L. ;
Riar, Jehan ;
Keil, Meg ;
Stratakis, Constantine A. .
PEDIATRICS, 2007, 120 (03) :E575-E586
[7]
Congenital central hypoventilation syndrome -: PHOX2B mutations and phenotype [J].
Berry-Kravis, Elizabeth M. ;
Zhou, Lili ;
Rand, Casey M. ;
Weese-Mayer, Debra E. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (10) :1139-1144
[8]
Hyperleptinaemia is associated with impaired gonadotrophin response to GnRH during late puberty in obese girls, not boys [J].
Bouvattier, C ;
Lahlou, N ;
Roger, M ;
Bougneres, P .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1998, 138 (06) :653-658
[9]
Obstructive sleep apnea syndrome in Prader-Willi syndrome: An unrecognized and untreated cause of cognitive and behavioral deficits? [J].
Camfferman, Danny ;
Lushington, Kurt ;
O'Donoghue, Fergal ;
McEvoy, R. Doug .
NEUROPSYCHOLOGY REVIEW, 2006, 16 (03) :123-129
[10]
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction [J].
Clément, K ;
Vaisse, C ;
Lahlou, N ;
Cabrol, S ;
Pelloux, V ;
Cassuto, D ;
Gourmelen, M ;
Dina, C ;
Chambaz, J ;
Lacorte, JM ;
Basdevant, A ;
Bougneres, P ;
Lebouc, Y ;
Froguel, P ;
Guy-Grand, B .
NATURE, 1998, 392 (6674) :398-401