Haberland syndrome: A very rare case report
Haberland syndrome, also known as encephalocraniocutaneous lipomatosis, is a rare, congenital neurocutaneous disorder. It is characterized by unilateral central nervous system, cutaneous, and ocular anomalies. We report here a case of 28-year-old female presented with history of intermittent episode...
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2016-01-01
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| Series: | Indian Journal of Health Sciences and Biomedical Research KLEU |
| Subjects: | |
| Online Access: | http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2016;volume=9;issue=3;spage=328;epage=330;aulast=Shah |
| _version_ | 1819047293735665664 |
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| author | Dhrumil J Shah Rishabh Gupta Bhagirath B Solanki |
| author_facet | Dhrumil J Shah Rishabh Gupta Bhagirath B Solanki |
| author_sort | Dhrumil J Shah |
| collection | DOAJ |
| description | Haberland syndrome, also known as encephalocraniocutaneous lipomatosis, is a rare, congenital neurocutaneous disorder. It is characterized by unilateral central nervous system, cutaneous, and ocular anomalies. We report here a case of 28-year-old female presented with history of intermittent episodes of generalized tonic–clonic type convulsions for 3 years, soft lipomatous swelling over the right temporal area with nonscarring alopecia of the part of frontal and parietal region, and ipsilateral scleral dermoid. Computed tomography findings were lipomas and calcification of falx. Magnetic resonance imaging showed right-sided hemiatrophy, two intracranial cysts, and enlargement of the right lateral ventricle. We report this case because of its rarity. |
| first_indexed | 2024-12-21T10:58:04Z |
| format | Article |
| id | doaj.art-4d9663d5bc03443cb705ccde5b6f0c94 |
| institution | Directory Open Access Journal |
| issn | 2542-6214 2542-6222 |
| language | English |
| last_indexed | 2024-12-21T10:58:04Z |
| publishDate | 2016-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Indian Journal of Health Sciences and Biomedical Research KLEU |
| spelling | doaj.art-4d9663d5bc03443cb705ccde5b6f0c942022-12-21T19:06:26ZengWolters Kluwer Medknow PublicationsIndian Journal of Health Sciences and Biomedical Research KLEU2542-62142542-62222016-01-019332833010.4103/2349-5006.196333Haberland syndrome: A very rare case reportDhrumil J ShahRishabh GuptaBhagirath B SolankiHaberland syndrome, also known as encephalocraniocutaneous lipomatosis, is a rare, congenital neurocutaneous disorder. It is characterized by unilateral central nervous system, cutaneous, and ocular anomalies. We report here a case of 28-year-old female presented with history of intermittent episodes of generalized tonic–clonic type convulsions for 3 years, soft lipomatous swelling over the right temporal area with nonscarring alopecia of the part of frontal and parietal region, and ipsilateral scleral dermoid. Computed tomography findings were lipomas and calcification of falx. Magnetic resonance imaging showed right-sided hemiatrophy, two intracranial cysts, and enlargement of the right lateral ventricle. We report this case because of its rarity.http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2016;volume=9;issue=3;spage=328;epage=330;aulast=ShahEncephalocraniocutaneous lipomatosisFishman syndromelipomatosisneurocutaneous disorder |
| spellingShingle | Dhrumil J Shah Rishabh Gupta Bhagirath B Solanki Haberland syndrome: A very rare case report Indian Journal of Health Sciences and Biomedical Research KLEU Encephalocraniocutaneous lipomatosis Fishman syndrome lipomatosis neurocutaneous disorder |
| title | Haberland syndrome: A very rare case report |
| title_full | Haberland syndrome: A very rare case report |
| title_fullStr | Haberland syndrome: A very rare case report |
| title_full_unstemmed | Haberland syndrome: A very rare case report |
| title_short | Haberland syndrome: A very rare case report |
| title_sort | haberland syndrome a very rare case report |
| topic | Encephalocraniocutaneous lipomatosis Fishman syndrome lipomatosis neurocutaneous disorder |
| url | http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2016;volume=9;issue=3;spage=328;epage=330;aulast=Shah |
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