Chediak-Higashi Syndrome (CHS)

Alias:
Chédiak-Higashi Syndrome
Chs
Oculocutaneous Albinism with Leukocyte Defect
Chediak-Steinbrinck-Higashi Syndrome
Chédiak-Higashi-Steinbrink Syndrome
Chediak-Higashi-Steinbrink Syndrome
Chediak - Steinbrinck Anomaly
Chédiak-Higashi Disease
Chediak-Higashi Disease
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Basic Information
Medical Symptom
Gene & Mutation
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Disease Model
References Literature
Chediak-Higashi Syndrome, also known as chédiak-higashi syndrome, is related to albinism and oculocutaneous albinism, and has symptoms including icterus, seizures and tremor. An important gene associated with Chediak-Higashi Syndrome is LYST (Lysosomal Trafficking Regulator), and among its related pathways/superpathways are NF-kappaB Signaling and GPR143 in melanocytes and retinal pigment epithelium cells. The drugs Busulfan and Cyclophosphamide have been mentioned in the context of this disorder. Affiliated tissues include skin and eye, and related phenotypes are abnormal leukocyte morphology and recurrent infections
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Basic Information

Inheritance
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Related Gene
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Reference
MALACARDS
AR
Child
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37
747
117

Medical Symptom

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Gene & Mutation

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References Literature

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