Document Detail

Prenatal dolichocephaly: Sign of trouble? -A variant of Miller-Dieker syndrome.
MedLine Citation:
PMID:  23301919     Owner:  NLM     Status:  Publisher    
Neuroimaging and molecular cytogenetics were used to ascertain the cause of disability in a case. The case was diagnosed to be a variant of Miller-Dieker syndrome (MDS). Retrospective analysis showed a prenatal scan reporting dolichocephaly. We evaluated dolichocephaly, the name associated with a nonsynostotic cause to be a physiological variant having no prognostic value, to that of a similar synostotic or secondary to a neurological disorder cause, with prognostic significance. The report confirmed early craniosynostosis in cases suspected with a neurological disorder and also on an important criterion in molecular testing strategy in cases suspected with MDS.
Tomy Kochuvareed Mampilly; George Tomy Mampilly; Neeradha Chandramohan; Murugan Velayutham; Jayesh Sheth; Frenny Sheth; Vijayalakshmy Janaki
Related Documents :
11481699 - Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a ...
8739439 - Oculopharyngeal muscular dystrophy in norway. survey of a large norwegian family.
23301919 - Prenatal dolichocephaly: sign of trouble? -a variant of miller-dieker syndrome.
12923869 - Blepharocheilodontic (bcd) syndrome: expanding the phenotype?
3825509 - Some problems of the systemic degeneration and atrophies.
16419129 - Familial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia.
18589409 - Left hand tactile agnosia after posterior callosal lesion.
24262449 - A large series of immunohistochemically confirmed cases of congenital muscular dystroph...
15669819 - Use of the leksell gamma knife c with automatic positioning system for the treatment of...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-1-10
Journal Detail:
Title:  Fetal and pediatric pathology     Volume:  -     ISSN:  1551-3823     ISO Abbreviation:  Fetal Pediatr Pathol     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-1-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101230972     Medline TA:  Fetal Pediatr Pathol     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
National Institute for Empowerment of Persons with Multiple Disabilities, Physical Medicine & Rehabilitation, ECR, Muttukadu, Kovalam Post , Chennai , India.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Osteogenesis imperfecta due to compound heterozygosity for the LEPRE1 gene.
Next Document:  Gas-Phase Azide Functionalization of Carbon.