Infantile spasms and developmental delay: A case of miller–Dieker syndrome
Background: Miller–Dieker syndrome (MDS) is a rare genetic disorder, due to contiguous gene deletion on chromosome 17p13.3, characterized by classical type I lissencephaly, severe developmental delay, seizures, cardiac defects, and dysmorphisms. West syndrome is a severe form of epilepsy with epilep...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Wolters Kluwer Medknow Publications
2023-01-01
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| Sarja: | Indian Pediatrics Case Reports |
| Aiheet: | |
| Linkit: | http://www.ipcares.org/article.asp?issn=2772-5170;year=2023;volume=3;issue=4;spage=225;epage=228;aulast= |
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