Neurodegeneration and Seizures Due to Copper Transport Defect (NSCT)

Alias:
Nsct
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Neurodegeneration and Seizures Due to Copper Transport Defect, also known as nsct, is related to intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies and polykaryocytosis inducer. An important gene associated with Neurodegeneration and Seizures Due to Copper Transport Defect is SLC31A1 (Solute Carrier Family 31 Member 1). Affiliated tissues include brain and skin, and related phenotypes are seizure and hyperreflexia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
8
2

Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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