Silver hair in a neonate: a tale of 2 fatal cases
Abstract Silver hair in a neonate is an uncommon occurrence. The aetiology of this condition is varied and is associated with immunodeficiency disorders such as Griscelli syndrome and Chédiak-Higashi syndrome. A preterm neonate with Griscelli syndrome type 2 might present with just silver colour sta...
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Veröffentlicht in: | Oxford Medical Case Reports 2024-09, Vol.2024 (9), p.omae106 |
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creator | Kumar, Lakshmi Satish Raghavendra, Prashanth Ranya Nair, Sruthi Vijaya Nathan D, Muthu Bargir, Umair Ahmed Haribalakrishna, Anitha Mahajan, Sunanda Arun |
description | Abstract
Silver hair in a neonate is an uncommon occurrence. The aetiology of this condition is varied and is associated with immunodeficiency disorders such as Griscelli syndrome and Chédiak-Higashi syndrome. A preterm neonate with Griscelli syndrome type 2 might present with just silver colour staining of hair including the lanugo hair with no other complications. In those with associated systemic abnormalities such as congenital pulmonary airway malformation, further evaluation for conditions such as Menke-Kinke hair syndrome is required. In this case series, we describe two unique cases of silver hair syndrome in preterm neonates with their clinical description, course in the hospital, role of hair mount and genetic testing for further identification and diagnosis of this disorder. |
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Silver hair in a neonate is an uncommon occurrence. The aetiology of this condition is varied and is associated with immunodeficiency disorders such as Griscelli syndrome and Chédiak-Higashi syndrome. A preterm neonate with Griscelli syndrome type 2 might present with just silver colour staining of hair including the lanugo hair with no other complications. In those with associated systemic abnormalities such as congenital pulmonary airway malformation, further evaluation for conditions such as Menke-Kinke hair syndrome is required. In this case series, we describe two unique cases of silver hair syndrome in preterm neonates with their clinical description, course in the hospital, role of hair mount and genetic testing for further identification and diagnosis of this disorder.</description><identifier>ISSN: 2053-8855</identifier><identifier>EISSN: 2053-8855</identifier><identifier>DOI: 10.1093/omcr/omae106</identifier><identifier>PMID: 39281335</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Genetic disorders ; Infants (Premature) ; Neonatology</subject><ispartof>Oxford Medical Case Reports, 2024-09, Vol.2024 (9), p.omae106</ispartof><rights>The Author(s) 2024. Published by Oxford University Press. 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press.</rights><rights>COPYRIGHT 2024 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c315t-9af1d8442485be8131914d02c751e02b22679e3120017f0368bbdc96a7eb0e903</cites><orcidid>0000-0002-6136-1278 ; 0000-0002-1263-8197 ; 0009-0006-3051-5840 ; 0000-0002-5767-6517</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,865,1605,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39281335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, Lakshmi Satish</creatorcontrib><creatorcontrib>Raghavendra, Prashanth Ranya</creatorcontrib><creatorcontrib>Nair, Sruthi</creatorcontrib><creatorcontrib>Vijaya Nathan D, Muthu</creatorcontrib><creatorcontrib>Bargir, Umair Ahmed</creatorcontrib><creatorcontrib>Haribalakrishna, Anitha</creatorcontrib><creatorcontrib>Mahajan, Sunanda Arun</creatorcontrib><title>Silver hair in a neonate: a tale of 2 fatal cases</title><title>Oxford Medical Case Reports</title><addtitle>Oxf Med Case Reports</addtitle><description>Abstract
Silver hair in a neonate is an uncommon occurrence. The aetiology of this condition is varied and is associated with immunodeficiency disorders such as Griscelli syndrome and Chédiak-Higashi syndrome. A preterm neonate with Griscelli syndrome type 2 might present with just silver colour staining of hair including the lanugo hair with no other complications. In those with associated systemic abnormalities such as congenital pulmonary airway malformation, further evaluation for conditions such as Menke-Kinke hair syndrome is required. In this case series, we describe two unique cases of silver hair syndrome in preterm neonates with their clinical description, course in the hospital, role of hair mount and genetic testing for further identification and diagnosis of this disorder.</description><subject>Genetic disorders</subject><subject>Infants (Premature)</subject><subject>Neonatology</subject><issn>2053-8855</issn><issn>2053-8855</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kEtLAzEUhYMottTuXEt2unBqHvNI3JXiCwou1HXIZG40MjOpyVTw35syVVxJIDmE79577kHolJIFJZJf-c6EdGmgpDxAU0YKnglRFId_9ATNY3wnhFBeUi7EMZpwyQTlvJgi-uTaTwj4TbuAXY817sH3eoDrJAfdAvYWM2x10tjoCPEEHVndRpjv3xl6ub15Xt1n68e7h9VynRlOiyGT2tJG5DnLRVFDmkYlzRvCTFVQIKxmrKwkcMqSr8oSXoq6bowsdQU1AUn4DF2MfTfBf2whDqpz0UDb6uRwGxVPKxNepYUSuhjR12RYud76IWiTTgOdM74H69L_UtBc5DJVpILLscAEH2MAqzbBdTp8KUrULli1C1btg0342d7Ktu6g-YV_YkzA-Qj47eb_Vt-Nfn5Y</recordid><startdate>202409</startdate><enddate>202409</enddate><creator>Kumar, Lakshmi Satish</creator><creator>Raghavendra, Prashanth Ranya</creator><creator>Nair, Sruthi</creator><creator>Vijaya Nathan D, Muthu</creator><creator>Bargir, Umair Ahmed</creator><creator>Haribalakrishna, Anitha</creator><creator>Mahajan, Sunanda Arun</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6136-1278</orcidid><orcidid>https://orcid.org/0000-0002-1263-8197</orcidid><orcidid>https://orcid.org/0009-0006-3051-5840</orcidid><orcidid>https://orcid.org/0000-0002-5767-6517</orcidid></search><sort><creationdate>202409</creationdate><title>Silver hair in a neonate: a tale of 2 fatal cases</title><author>Kumar, Lakshmi Satish ; Raghavendra, Prashanth Ranya ; Nair, Sruthi ; Vijaya Nathan D, Muthu ; Bargir, Umair Ahmed ; Haribalakrishna, Anitha ; Mahajan, Sunanda Arun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-9af1d8442485be8131914d02c751e02b22679e3120017f0368bbdc96a7eb0e903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Genetic disorders</topic><topic>Infants (Premature)</topic><topic>Neonatology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Lakshmi Satish</creatorcontrib><creatorcontrib>Raghavendra, Prashanth Ranya</creatorcontrib><creatorcontrib>Nair, Sruthi</creatorcontrib><creatorcontrib>Vijaya Nathan D, Muthu</creatorcontrib><creatorcontrib>Bargir, Umair Ahmed</creatorcontrib><creatorcontrib>Haribalakrishna, Anitha</creatorcontrib><creatorcontrib>Mahajan, Sunanda Arun</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>MEDLINE - Academic</collection><jtitle>Oxford Medical Case Reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Lakshmi Satish</au><au>Raghavendra, Prashanth Ranya</au><au>Nair, Sruthi</au><au>Vijaya Nathan D, Muthu</au><au>Bargir, Umair Ahmed</au><au>Haribalakrishna, Anitha</au><au>Mahajan, Sunanda Arun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Silver hair in a neonate: a tale of 2 fatal cases</atitle><jtitle>Oxford Medical Case Reports</jtitle><addtitle>Oxf Med Case Reports</addtitle><date>2024-09</date><risdate>2024</risdate><volume>2024</volume><issue>9</issue><spage>omae106</spage><pages>omae106-</pages><issn>2053-8855</issn><eissn>2053-8855</eissn><abstract>Abstract
Silver hair in a neonate is an uncommon occurrence. The aetiology of this condition is varied and is associated with immunodeficiency disorders such as Griscelli syndrome and Chédiak-Higashi syndrome. A preterm neonate with Griscelli syndrome type 2 might present with just silver colour staining of hair including the lanugo hair with no other complications. In those with associated systemic abnormalities such as congenital pulmonary airway malformation, further evaluation for conditions such as Menke-Kinke hair syndrome is required. In this case series, we describe two unique cases of silver hair syndrome in preterm neonates with their clinical description, course in the hospital, role of hair mount and genetic testing for further identification and diagnosis of this disorder.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>39281335</pmid><doi>10.1093/omcr/omae106</doi><orcidid>https://orcid.org/0000-0002-6136-1278</orcidid><orcidid>https://orcid.org/0000-0002-1263-8197</orcidid><orcidid>https://orcid.org/0009-0006-3051-5840</orcidid><orcidid>https://orcid.org/0000-0002-5767-6517</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford Journals Open Access Collection; PubMed Central |
subjects | Genetic disorders Infants (Premature) Neonatology |
title | Silver hair in a neonate: a tale of 2 fatal cases |
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