Unusual facial lesions in H syndrome

Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histologic...
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Autor*in:	Mariem Rekik [verfasserIn] Emna Bahloul [verfasserIn] Mohamed Ben Rejeb [verfasserIn] Khadija Sellami [verfasserIn] Slim Charfi [verfasserIn] Hamza Chouk [verfasserIn] Tahya Boudaouara [verfasserIn] Hamida Turki [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis

Übergeordnetes Werk:	In: Clinical Case Reports - Wiley, 2013, 10(2022), 7, Seite n/a-n/a
Übergeordnetes Werk:	volume:10 ; year:2022 ; number:7 ; pages:n/a-n/a

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1002/ccr3.6098

Katalog-ID:	DOAJ032948654

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520			\|a Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis.
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publishDate	2022
allfields	10.1002/ccr3.6098 doi (DE-627)DOAJ032948654 (DE-599)DOAJ38d7f46264044549b55b645b499bdee1 DE-627 ger DE-627 rakwb eng R5-920 Mariem Rekik verfasserin aut Unusual facial lesions in H syndrome 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis Medicine R Medicine (General) Emna Bahloul verfasserin aut Mohamed Ben Rejeb verfasserin aut Khadija Sellami verfasserin aut Slim Charfi verfasserin aut Hamza Chouk verfasserin aut Tahya Boudaouara verfasserin aut Hamida Turki verfasserin aut In Clinical Case Reports Wiley, 2013 10(2022), 7, Seite n/a-n/a (DE-627)771392567 (DE-600)2740234-4 20500904 nnns volume:10 year:2022 number:7 pages:n/a-n/a https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/article/38d7f46264044549b55b645b499bdee1 kostenfrei https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/toc/2050-0904 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2022 7 n/a-n/a
spelling	10.1002/ccr3.6098 doi (DE-627)DOAJ032948654 (DE-599)DOAJ38d7f46264044549b55b645b499bdee1 DE-627 ger DE-627 rakwb eng R5-920 Mariem Rekik verfasserin aut Unusual facial lesions in H syndrome 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis Medicine R Medicine (General) Emna Bahloul verfasserin aut Mohamed Ben Rejeb verfasserin aut Khadija Sellami verfasserin aut Slim Charfi verfasserin aut Hamza Chouk verfasserin aut Tahya Boudaouara verfasserin aut Hamida Turki verfasserin aut In Clinical Case Reports Wiley, 2013 10(2022), 7, Seite n/a-n/a (DE-627)771392567 (DE-600)2740234-4 20500904 nnns volume:10 year:2022 number:7 pages:n/a-n/a https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/article/38d7f46264044549b55b645b499bdee1 kostenfrei https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/toc/2050-0904 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2022 7 n/a-n/a
allfields_unstemmed	10.1002/ccr3.6098 doi (DE-627)DOAJ032948654 (DE-599)DOAJ38d7f46264044549b55b645b499bdee1 DE-627 ger DE-627 rakwb eng R5-920 Mariem Rekik verfasserin aut Unusual facial lesions in H syndrome 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis Medicine R Medicine (General) Emna Bahloul verfasserin aut Mohamed Ben Rejeb verfasserin aut Khadija Sellami verfasserin aut Slim Charfi verfasserin aut Hamza Chouk verfasserin aut Tahya Boudaouara verfasserin aut Hamida Turki verfasserin aut In Clinical Case Reports Wiley, 2013 10(2022), 7, Seite n/a-n/a (DE-627)771392567 (DE-600)2740234-4 20500904 nnns volume:10 year:2022 number:7 pages:n/a-n/a https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/article/38d7f46264044549b55b645b499bdee1 kostenfrei https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/toc/2050-0904 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2022 7 n/a-n/a
allfieldsGer	10.1002/ccr3.6098 doi (DE-627)DOAJ032948654 (DE-599)DOAJ38d7f46264044549b55b645b499bdee1 DE-627 ger DE-627 rakwb eng R5-920 Mariem Rekik verfasserin aut Unusual facial lesions in H syndrome 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis Medicine R Medicine (General) Emna Bahloul verfasserin aut Mohamed Ben Rejeb verfasserin aut Khadija Sellami verfasserin aut Slim Charfi verfasserin aut Hamza Chouk verfasserin aut Tahya Boudaouara verfasserin aut Hamida Turki verfasserin aut In Clinical Case Reports Wiley, 2013 10(2022), 7, Seite n/a-n/a (DE-627)771392567 (DE-600)2740234-4 20500904 nnns volume:10 year:2022 number:7 pages:n/a-n/a https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/article/38d7f46264044549b55b645b499bdee1 kostenfrei https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/toc/2050-0904 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2022 7 n/a-n/a
allfieldsSound	10.1002/ccr3.6098 doi (DE-627)DOAJ032948654 (DE-599)DOAJ38d7f46264044549b55b645b499bdee1 DE-627 ger DE-627 rakwb eng R5-920 Mariem Rekik verfasserin aut Unusual facial lesions in H syndrome 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis. dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis Medicine R Medicine (General) Emna Bahloul verfasserin aut Mohamed Ben Rejeb verfasserin aut Khadija Sellami verfasserin aut Slim Charfi verfasserin aut Hamza Chouk verfasserin aut Tahya Boudaouara verfasserin aut Hamida Turki verfasserin aut In Clinical Case Reports Wiley, 2013 10(2022), 7, Seite n/a-n/a (DE-627)771392567 (DE-600)2740234-4 20500904 nnns volume:10 year:2022 number:7 pages:n/a-n/a https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/article/38d7f46264044549b55b645b499bdee1 kostenfrei https://doi.org/10.1002/ccr3.6098 kostenfrei https://doaj.org/toc/2050-0904 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2022 7 n/a-n/a
language	English
source	In Clinical Case Reports 10(2022), 7, Seite n/a-n/a volume:10 year:2022 number:7 pages:n/a-n/a
sourceStr	In Clinical Case Reports 10(2022), 7, Seite n/a-n/a volume:10 year:2022 number:7 pages:n/a-n/a
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis Medicine R Medicine (General)
isfreeaccess_bool	true
container_title	Clinical Case Reports
authorswithroles_txt_mv	Mariem Rekik @@aut@@ Emna Bahloul @@aut@@ Mohamed Ben Rejeb @@aut@@ Khadija Sellami @@aut@@ Slim Charfi @@aut@@ Hamza Chouk @@aut@@ Tahya Boudaouara @@aut@@ Hamida Turki @@aut@@
publishDateDaySort_date	2022-01-01T00:00:00Z
hierarchy_top_id	771392567
id	DOAJ032948654
language_de	englisch
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callnumber-first	R - Medicine
author	Mariem Rekik
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topic_title	R5-920 Unusual facial lesions in H syndrome dermoscopy facial lesions H Syndrome non‐Langerhans cell histiocytosis
topic	misc R5-920 misc dermoscopy misc facial lesions misc H Syndrome misc non‐Langerhans cell histiocytosis misc Medicine misc R misc Medicine (General)
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title	Unusual facial lesions in H syndrome
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title_full	Unusual facial lesions in H syndrome
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title_sort	unusual facial lesions in h syndrome
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title_auth	Unusual facial lesions in H syndrome
abstract	Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis.
abstractGer	Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis.
abstract_unstemmed	Abstract H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non‐Langerhans cell histiocytosis.
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title_short	Unusual facial lesions in H syndrome
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Unusual facial lesions in H syndrome

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