| Massive cranial osteolysis, skin changes, growth retardation and developmental delay: Gorham syndrome with systemic manifestations? | |
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MedLine Citation:
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PMID: 20186788 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We report on a 16-month-old girl with multiple swellings on her skull due to massive osteolysis, growth retardation, facial anomalies, and wrinkly skin with mosaic hypopigmentation. She also had severe hypercalcemia, which gradually returned to normal levels. The condition likely represents Gorham syndrome with systemic manifestations. |
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Authors:
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K M Girisha; H K Ganesh; Lakshmi Rao; P S Srilatha |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: American journal of medical genetics. Part A Volume: 152A ISSN: 1552-4833 ISO Abbreviation: Am. J. Med. Genet. A Publication Date: 2010 Mar |
Date Detail:
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Created Date: 2010-03-01 Completed Date: 2010-04-12 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101235741 Medline TA: Am J Med Genet A Country: United States |
Other Details:
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Languages: eng Pagination: 759-63 Citation Subset: IM |
Copyright Information:
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(c) 2010 Wiley-Liss, Inc. |
Affiliation:
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Department of Pediatrics, Kasturba Medical College, Manipal, Karnataka, India. girishkatta@gmail.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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genetics* Developmental Disabilities / genetics* Female Growth Disorders / genetics* Humans Hypopigmentation / genetics Infant Osteolysis, Essential / genetics*, pathology* Skin Abnormalities / genetics, pathology Skull / pathology* Syndrome |
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