Congenital central hypoventilation syndrome and hypoglycaemia.
Acta Paediatr
; 101(2): e92-6, 2012 Feb.
Article
en En
| MEDLINE
| ID: mdl-22103583
ABSTRACT
UNLABELLED Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder typically presenting in infants with an impaired automatic control of breathing, particularly during sleep, and often associated with variable patterns of autonomic nervous system dysregulations. We studied three children who had CCHS associated with episodes of severe hypoglycaemia and hyperinsulinaemia; we discuss the possible relationship with impaired dopamine-beta-hydroxylase function. CONCLUSION:
Hypoglycaemia and hyperinsulinaemia might be suspected in children with CCHS presenting with seizures and hyperhydrosis; though, further studies are needed to confirm this association.
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Apnea Central del Sueño
/
Hiperinsulinismo
/
Hipoglucemia
/
Hipoventilación
Tipo de estudio:
Etiology_studies
Límite:
Humans
/
Infant
/
Male
Idioma:
En
Revista:
Acta Paediatr
Año:
2012
Tipo del documento:
Article
País de afiliación:
Italia