Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum

C Ewenczyk, A Leroux, A Roubergue, V Laugel… - Brain, 2008 - academic.oup.com
C Ewenczyk, A Leroux, A Roubergue, V Laugel, A Afenjar, JM Saudubray, P Beauvais…
Brain, 2008academic.oup.com
Type II recessive hereditary methaemoglobinaemia (RHM) is a rare disease due to
generalized NADH-cytochrome b5 reductase (cytb5r) deficiency. It results in mild cyanosis
and severe neurological impairment. The clinical features and long-term outcome are poorly
documented, and there are no systematic reviews. We examined six cases of type II RHM,
four of which were new, together with 45 previously published cases, in order to establish
the range of phenotypic expression. The clinical picture was very similar in most cases, with …
Abstract
Type II recessive hereditary methaemoglobinaemia (RHM) is a rare disease due to generalized NADH-cytochrome b5 reductase (cytb5r) deficiency. It results in mild cyanosis and severe neurological impairment. The clinical features and long-term outcome are poorly documented, and there are no systematic reviews. We examined six cases of type II RHM, four of which were new, together with 45 previously published cases, in order to establish the range of phenotypic expression. The clinical picture was very similar in most cases, with severe encephalopathy, microcephaly, generalized dystonia, movement disorders and mild cyanosis. The neurological prognosis was poor; in particular, none of the patients walked or spoke. In addition, the possibility of an atypical and milder phenotype was considered. We concluded that children with unexplained severe encephalopathy associated with generalized dystonia should be examined for cyanosis and have a methaemoglobinaemia assay performed. The diagnosis can be confirmed by very low cytb5r activity in both red and white blood cells. Here we report three novel mutations in the NADH-cytochrome b5 reductase gene. Prenatal diagnosis of this extremely severe disease should be proposed to affected families.
Oxford University Press