Lissencephaly 3

Common Name(s)

Lissencephaly 3

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Lissencephaly 3" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Lissencephaly 3" returned 6 free, full-text research articles on human participants. First 3 results:

Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.
 

Author(s): Chin-Yi Lin, Chih-Ping Chen, Chiung-Ling Liau, Pen-Hua Su, Teng-Fu Tsao, Tung-Yao Chang, Wayseen Wang

Journal: Taiwan J Obstet Gynecol. 2009 Dec;48(4):408-11.

 

To present the prenatal magnetic resonance imaging (MRI) and ultrasound findings of Miller-Dieker lissencephaly syndrome (MDLS) associated with chromosome 17p13.3 deletion in a fetus.

Last Updated: 4 Jan 2010

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Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation.
 

Author(s): Salvatore Grosso, Marco Fichera, Ornella Galesi, Daniela Luciano, Lucia Pucci, Francesca Giardini, Rosario Berardi, Paolo Balestri

Journal: Dev Med Child Neurol. 2008 Jun;50(6):473-6.

 

Periventricular nodular heterotopia and Miller-Dieker syndrome are two different disorders of brain development. Miller-Dieker syndrome exhibits classical lissencephaly and is related to defects in the lissencephaly gene (LIS1). Periventricular nodular heterotopia is characterized ...

Last Updated: 20 May 2008

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Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3.
 

Author(s): Carlos Cardoso, Richard J Leventer, Heather L Ward, Kazuhito Toyo-Oka, June Chung, Alyssa Gross, Christa L Martin, Judith Allanson, Daniela T Pilz, Ann H Olney, Osvaldo M Mutchinick, Shinji Hirotsune, Anthony Wynshaw-Boris, William B Dobyns, David H Ledbetter

Journal: Am. J. Hum. Genet.. 2003 Apr;72(4):918-30.

 

Deletions of 17p13.3, including the LIS1 gene, result in the brain malformation lissencephaly, which is characterized by reduced gyration and cortical thickening; however, the phenotype can vary from isolated lissencephaly sequence (ILS) to Miller-Dieker syndrome (MDS). At the clinical ...

Last Updated: 21 Mar 2003

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Reviews from the PubMed Database

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The terms "Lissencephaly 3" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.