Seckel syndrome 2

Common Name(s)

Seckel syndrome 2

Seckel syndrome is a rare autosomal recessive disorder characterized by growth retardation, microcephaly with mental retardation, and a characteristic facial appearance ({1:Borglum et al., 2001}). For a general phenotypic description and a discussion of genetic heterogeneity of Seckel syndrome, see SCKL1 ({210600}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Seckel syndrome 2" for support, advocacy or research.

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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 "Seckel syndrome 2" returned 1 free, full-text research articles on human participants. First 3 results:

A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
 

Author(s): A D Børglum, T Balslev, A Haagerup, N Birkebaek, H Binderup, T A Kruse, J M Hertz

Journal: Eur. J. Hum. Genet.. 2001 Oct;9(10):753-7.

 

Seckel syndrome (MIM 210600) is a rare autosomal recessive disorder with a heterogeneous appearance. Key features are growth retardation, microcephaly with mental retardation, and a characteristic 'bird-headed' facial appearance. We have performed a genome-wide linkage scan in a consanguineous ...

Last Updated: 8 Jan 2002

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The terms "Seckel syndrome 2" returned 0 free, full-text review articles on human participants.

 
 
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