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Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene

Histamine is involved in various physiological functions like sleep–wake cycle and stress regulation. The histamine N-methyltransferase (HNMT) enzyme is the only pathway for termination of histamine neurotransmission in the central nervous system. Experiments with HNMT knockout mice generated aggres...

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Published in:BMJ case reports 2020-12, Vol.13 (12), p.e235972
Main Authors: Verhoeven, Willem M A, Egger, Jos I M, Janssen, Paddy K C, van Haeringen, Arie
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description Histamine is involved in various physiological functions like sleep–wake cycle and stress regulation. The histamine N-methyltransferase (HNMT) enzyme is the only pathway for termination of histamine neurotransmission in the central nervous system. Experiments with HNMT knockout mice generated aggressive behaviours and dysregulation of sleep–wake cycles. Recently, seven members of two unrelated consanguineous families have been reported in whom two different missense HNMT mutations were identified. All showed severe intellectual disability, delayed speech development and mild regression from the age of 5 years without, however, any dysmorphisms or congenital abnormality. A diagnosis of mental retardation, autosomal recessive 51 was made. Here, we describe a severely mentally retarded adolescent male born from second cousins with a homozygous mutation in HNMT. His phenotypic profile comprised aggression, delayed speech, autism, sleep disturbances and gastro-intestinal problems. At early age, regression occurred. Treatment with hydroxyzine combined with a histamine-restricted diet resulted in significant general improvement.
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subjects Age
Aggression - physiology
Autism
Behavior
Brain - metabolism
Case reports
Child & adolescent psychiatry
Congenital diseases
genetics
Hematology
Histamine
Histamine - metabolism
Histamine N-Methyltransferase - genetics
Histamine N-Methyltransferase - metabolism
Homocysteine
Homozygote
Humans
Hydroxyzine - therapeutic use
Intellectual disabilities
Intellectual Disability - diet therapy
Intellectual Disability - drug therapy
Intellectual Disability - genetics
Intellectual Disability - metabolism
Male
metabolic disorders
Mutation
Parents & parenting
Patients
psychiatry (drugs and medicines)
Rare Disease
Sleep
Sleep - physiology
Teenagers
therapeutic indications
Treatment Outcome
Urine
Young Adult
title Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene
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