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GTR Home > Conditions/Phenotypes > Dias-Logan syndrome

Dias-Logan syndrome

Synonyms
INTELLECTUAL DEVELOPMENTAL DISORDER WITH HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN; Intellectual developmental disorder with persistence of fetal hemoglobin

Summary

Excerpted from the GeneReview: BCL11A-Related Intellectual Disability
BCL11A-related intellectual disability (BCL11A-ID) is characterized by developmental delay / intellectual disability of variable degree, neonatal hypotonia, microcephaly, distinctive but variable facial characteristics, behavior problems, and asymptomatic persistence of fetal hemoglobin. Growth delay, seizures, and autism spectrum disorder have also been reported in some affected individuals.
Full text of GeneReview (by section):
Summary
Diagnosis
Clinical Characteristics
Genetically Related (Allelic) Disorders
Differential Diagnosis
Management
Genetic Counseling
Resources
Molecular Genetics
Chapter Notes
References
Authors:
Angela Peron
Kimberley Bradbury
David H Viskochil
view full author information

Available tests

12 tests are in the database for this condition.

Clinical tests (12 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CTIP1, DILOS, EVI9, HBFQTL5, SMARCM1, ZNF856, BCL11A
    Summary: BCL11 transcription factor A

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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