ROHHAD syndrome - A still unrecognized cause of childhood obesity: report of three cases.
ROHHAD syndrome
autonomic dysregulation
children
hypothalamic dysfunction
hypoventilation
obesity
Journal
Journal of pediatric endocrinology & metabolism : JPEM
ISSN: 2191-0251
Titre abrégé: J Pediatr Endocrinol Metab
Pays: Germany
ID NLM: 9508900
Informations de publication
Date de publication:
30 Sep 2020
30 Sep 2020
Historique:
received:
22
03
2020
accepted:
09
07
2020
entrez:
29
9
2020
pubmed:
30
9
2020
medline:
16
6
2021
Statut:
epublish
Résumé
Objectives Rapid-onset obesity with hypoventilation, hypothalamic dysfunction, and autonomic dysregulation (ROHHAD) is a rare, potentially fatal, pediatric syndrome. Case presentations We describe three cases of ROHHAD-syndrome in Greece. The main and earliest symptom was the excessive and rapid weight gain at 5, 2, and 3 years of age. Years after the onset of obesity, the patients developed hypothalamic dysfunction with various endocrinological abnormalities (at 9, 8, and 6.8 years, respectively), autonomic dysregulation and finally, alveolar hypoventilation (at 14.6, 8, and 7.8 years, respectively), leading to the diagnosis of ROHHAD-syndrome. Conclusions The rarity of the syndrome, the variable symptoms' presentation, and the lack of specific diagnostic tests could explain why no previous cases have been reported from our country. The rapid onset of obesity was underestimated, and the patients were misdiagnosed with other more common obesity syndromes. Therefore, we propose a questionnaire to help physicians identify patients with ROHHAD-syndrome.
Identifiants
pubmed: 32990648
doi: 10.1515/jpem-2020-0111
pii: /j/jpem.2020.33.issue-10/jpem-2020-0111/jpem-2020-0111.xml
doi:
pii:
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM