Loading…
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...
Saved in:
Published in: | BMJ case reports 2020-12, Vol.13 (12), p.e235972 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3 |
---|---|
cites | cdi_FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3 |
container_end_page | |
container_issue | 12 |
container_start_page | e235972 |
container_title | BMJ case reports |
container_volume | 13 |
creator | Verhoeven, Willem M A Egger, Jos I M Janssen, Paddy K C van Haeringen, Arie |
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. |
doi_str_mv | 10.1136/bcr-2020-235972 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7735107</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2469564061</sourcerecordid><originalsourceid>FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3</originalsourceid><addsrcrecordid>eNqNkc9LHDEUx0OpVFHPvUnAm2Vqfk5mLoJIrQWrF4XeQjJ5u5tlZrImGcv2rzeyurUHobm8kPd53_cNX4Q-U_KVUl6f2i5WjDBSMS5bxT6gPaqkqlRLfn18c99FhyktSTmcikbwT2iXc05Jw-Qemp-7qc94MD3glckexox_-7zACR4hAvZjhr6HLk-mx84nY33v8xp3ZkrgsF1jgxdhCH_W8zAlPEy5iISxzOG8AHx18_MOz2GEA7QzM32Cw5e6j-4vv91dXFXXt99_XJxfV1a0LFe8kW1jqWCMUqibugVqlXFyJoSlUrC2rWshjOCiMY5IQhhXrlGKOlvenOX76Gyju5rsAK4r_4mm16voBxPXOhiv_-2MfqHn4VErxSUlqggcvwjE8DBBynoZpjgWz5qJupW1IDUt1OmG6mJIKcJsu4ES_RyOLuHo53D0JpwycfTW2JZ_jaIAJxvADsv_UPvyF94afI9-AqpopTU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2469564061</pqid></control><display><type>article</type><title>Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene</title><source>NCBI_PubMed Central(免费)</source><creator>Verhoeven, Willem M A ; Egger, Jos I M ; Janssen, Paddy K C ; van Haeringen, Arie</creator><creatorcontrib>Verhoeven, Willem M A ; Egger, Jos I M ; Janssen, Paddy K C ; van Haeringen, Arie</creatorcontrib><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.</description><identifier>ISSN: 1757-790X</identifier><identifier>EISSN: 1757-790X</identifier><identifier>DOI: 10.1136/bcr-2020-235972</identifier><identifier>PMID: 33310825</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd</publisher><subject>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</subject><ispartof>BMJ case reports, 2020-12, Vol.13 (12), p.e235972</ispartof><rights>BMJ Publishing Group Limited 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2020 BMJ Publishing Group Limited 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>BMJ Publishing Group Limited 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3</citedby><cites>FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735107/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735107/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33310825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Verhoeven, Willem M A</creatorcontrib><creatorcontrib>Egger, Jos I M</creatorcontrib><creatorcontrib>Janssen, Paddy K C</creatorcontrib><creatorcontrib>van Haeringen, Arie</creatorcontrib><title>Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene</title><title>BMJ case reports</title><addtitle>BMJ Case Rep</addtitle><addtitle>BMJ Case Rep</addtitle><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.</description><subject>Age</subject><subject>Aggression - physiology</subject><subject>Autism</subject><subject>Behavior</subject><subject>Brain - metabolism</subject><subject>Case reports</subject><subject>Child & adolescent psychiatry</subject><subject>Congenital diseases</subject><subject>genetics</subject><subject>Hematology</subject><subject>Histamine</subject><subject>Histamine - metabolism</subject><subject>Histamine N-Methyltransferase - genetics</subject><subject>Histamine N-Methyltransferase - metabolism</subject><subject>Homocysteine</subject><subject>Homozygote</subject><subject>Humans</subject><subject>Hydroxyzine - therapeutic use</subject><subject>Intellectual disabilities</subject><subject>Intellectual Disability - diet therapy</subject><subject>Intellectual Disability - drug therapy</subject><subject>Intellectual Disability - genetics</subject><subject>Intellectual Disability - metabolism</subject><subject>Male</subject><subject>metabolic disorders</subject><subject>Mutation</subject><subject>Parents & parenting</subject><subject>Patients</subject><subject>psychiatry (drugs and medicines)</subject><subject>Rare Disease</subject><subject>Sleep</subject><subject>Sleep - physiology</subject><subject>Teenagers</subject><subject>therapeutic indications</subject><subject>Treatment Outcome</subject><subject>Urine</subject><subject>Young Adult</subject><issn>1757-790X</issn><issn>1757-790X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><recordid>eNqNkc9LHDEUx0OpVFHPvUnAm2Vqfk5mLoJIrQWrF4XeQjJ5u5tlZrImGcv2rzeyurUHobm8kPd53_cNX4Q-U_KVUl6f2i5WjDBSMS5bxT6gPaqkqlRLfn18c99FhyktSTmcikbwT2iXc05Jw-Qemp-7qc94MD3glckexox_-7zACR4hAvZjhr6HLk-mx84nY33v8xp3ZkrgsF1jgxdhCH_W8zAlPEy5iISxzOG8AHx18_MOz2GEA7QzM32Cw5e6j-4vv91dXFXXt99_XJxfV1a0LFe8kW1jqWCMUqibugVqlXFyJoSlUrC2rWshjOCiMY5IQhhXrlGKOlvenOX76Gyju5rsAK4r_4mm16voBxPXOhiv_-2MfqHn4VErxSUlqggcvwjE8DBBynoZpjgWz5qJupW1IDUt1OmG6mJIKcJsu4ES_RyOLuHo53D0JpwycfTW2JZ_jaIAJxvADsv_UPvyF94afI9-AqpopTU</recordid><startdate>20201212</startdate><enddate>20201212</enddate><creator>Verhoeven, Willem M A</creator><creator>Egger, Jos I M</creator><creator>Janssen, Paddy K C</creator><creator>van Haeringen, Arie</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20201212</creationdate><title>Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene</title><author>Verhoeven, Willem M A ; Egger, Jos I M ; Janssen, Paddy K C ; van Haeringen, Arie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Age</topic><topic>Aggression - physiology</topic><topic>Autism</topic><topic>Behavior</topic><topic>Brain - metabolism</topic><topic>Case reports</topic><topic>Child & adolescent psychiatry</topic><topic>Congenital diseases</topic><topic>genetics</topic><topic>Hematology</topic><topic>Histamine</topic><topic>Histamine - metabolism</topic><topic>Histamine N-Methyltransferase - genetics</topic><topic>Histamine N-Methyltransferase - metabolism</topic><topic>Homocysteine</topic><topic>Homozygote</topic><topic>Humans</topic><topic>Hydroxyzine - therapeutic use</topic><topic>Intellectual disabilities</topic><topic>Intellectual Disability - diet therapy</topic><topic>Intellectual Disability - drug therapy</topic><topic>Intellectual Disability - genetics</topic><topic>Intellectual Disability - metabolism</topic><topic>Male</topic><topic>metabolic disorders</topic><topic>Mutation</topic><topic>Parents & parenting</topic><topic>Patients</topic><topic>psychiatry (drugs and medicines)</topic><topic>Rare Disease</topic><topic>Sleep</topic><topic>Sleep - physiology</topic><topic>Teenagers</topic><topic>therapeutic indications</topic><topic>Treatment Outcome</topic><topic>Urine</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Verhoeven, Willem M A</creatorcontrib><creatorcontrib>Egger, Jos I M</creatorcontrib><creatorcontrib>Janssen, Paddy K C</creatorcontrib><creatorcontrib>van Haeringen, Arie</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>PHMC-Proquest健康医学期刊库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMJ case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Verhoeven, Willem M A</au><au>Egger, Jos I M</au><au>Janssen, Paddy K C</au><au>van Haeringen, Arie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene</atitle><jtitle>BMJ case reports</jtitle><stitle>BMJ Case Rep</stitle><addtitle>BMJ Case Rep</addtitle><date>2020-12-12</date><risdate>2020</risdate><volume>13</volume><issue>12</issue><spage>e235972</spage><pages>e235972-</pages><issn>1757-790X</issn><eissn>1757-790X</eissn><abstract>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.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd</pub><pmid>33310825</pmid><doi>10.1136/bcr-2020-235972</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1757-790X |
ispartof | BMJ case reports, 2020-12, Vol.13 (12), p.e235972 |
issn | 1757-790X 1757-790X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7735107 |
source | NCBI_PubMed Central(免费) |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T13%3A30%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Adult%20male%20patient%20with%20severe%20intellectual%20disability%20caused%20by%20a%20homozygous%20mutation%20in%20the%20HNMT%20gene&rft.jtitle=BMJ%20case%20reports&rft.au=Verhoeven,%20Willem%20M%20A&rft.date=2020-12-12&rft.volume=13&rft.issue=12&rft.spage=e235972&rft.pages=e235972-&rft.issn=1757-790X&rft.eissn=1757-790X&rft_id=info:doi/10.1136/bcr-2020-235972&rft_dat=%3Cproquest_pubme%3E2469564061%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b492t-38598b142211e6869e1b7ad5f44b1542996644a4348ad0500237d8771db434db3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2469564061&rft_id=info:pmid/33310825&rfr_iscdi=true |