Grönblad-Strandberg syndrome. Presentation of a patient
Syndrome Grönblad-Strandberg is a rare hereditary disease it is a genetic disorder of connective tissue characterized by fragmentation of elastic fibers and subsequent calcification affecting the dermis, blood vessels and Bruch's membrane of retina. The inheritance pattern is highly variable, m...
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | Spanish |
| Published: |
Editorial Ciencias Médicas
2014-06-01
|
| Series: | Acta Médica del Centro |
| Subjects: | |
| Online Access: | http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/134 |
| _version_ | 1811248508839133184 |
|---|---|
| author | Zoila Fariñas Falcón Rubén Antoliano Rangel Fleites Amarilis Hernández Camacho |
| author_facet | Zoila Fariñas Falcón Rubén Antoliano Rangel Fleites Amarilis Hernández Camacho |
| author_sort | Zoila Fariñas Falcón |
| collection | DOAJ |
| description | Syndrome Grönblad-Strandberg is a rare hereditary disease it is a genetic disorder of connective tissue characterized by fragmentation of elastic fibers and subsequent calcification affecting the dermis, blood vessels and Bruch's membrane of retina. The inheritance pattern is highly variable, making it possible that this disease may be underdiagnosed. The low incidence of this condition justifies the presentation of a case who suffered decreased vision in both eyes by macular atrophy and causes of low vision. |
| first_indexed | 2024-04-12T15:29:21Z |
| format | Article |
| id | doaj.art-8ffa073862fa41eda8157fecb2538554 |
| institution | Directory Open Access Journal |
| issn | 2709-7927 |
| language | Spanish |
| last_indexed | 2024-04-12T15:29:21Z |
| publishDate | 2014-06-01 |
| publisher | Editorial Ciencias Médicas |
| record_format | Article |
| series | Acta Médica del Centro |
| spelling | doaj.art-8ffa073862fa41eda8157fecb25385542022-12-22T03:27:09ZspaEditorial Ciencias MédicasActa Médica del Centro2709-79272014-06-0182102106125Grönblad-Strandberg syndrome. Presentation of a patientZoila Fariñas Falcón0Rubén Antoliano Rangel Fleites1Amarilis Hernández Camacho2Hospital Provincial Universitario “Arnaldo Milián Castro”, Santa Clara, Villa ClaraHospital Provincial Universitario “Arnaldo Milián Castro”, Santa Clara, Villa ClaraHospital Provincial Universitario “Arnaldo Milián Castro”, Santa Clara, Villa ClaraSyndrome Grönblad-Strandberg is a rare hereditary disease it is a genetic disorder of connective tissue characterized by fragmentation of elastic fibers and subsequent calcification affecting the dermis, blood vessels and Bruch's membrane of retina. The inheritance pattern is highly variable, making it possible that this disease may be underdiagnosed. The low incidence of this condition justifies the presentation of a case who suffered decreased vision in both eyes by macular atrophy and causes of low vision.http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/134seudoxantoma elástico |
| spellingShingle | Zoila Fariñas Falcón Rubén Antoliano Rangel Fleites Amarilis Hernández Camacho Grönblad-Strandberg syndrome. Presentation of a patient Acta Médica del Centro seudoxantoma elástico |
| title | Grönblad-Strandberg syndrome. Presentation of a patient |
| title_full | Grönblad-Strandberg syndrome. Presentation of a patient |
| title_fullStr | Grönblad-Strandberg syndrome. Presentation of a patient |
| title_full_unstemmed | Grönblad-Strandberg syndrome. Presentation of a patient |
| title_short | Grönblad-Strandberg syndrome. Presentation of a patient |
| title_sort | gronblad strandberg syndrome presentation of a patient |
| topic | seudoxantoma elástico |
| url | http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/134 |
| work_keys_str_mv | AT zoilafarinasfalcon gronbladstrandbergsyndromepresentationofapatient AT rubenantolianorangelfleites gronbladstrandbergsyndromepresentationofapatient AT amarilishernandezcamacho gronbladstrandbergsyndromepresentationofapatient |