Beare-Stevenson Cutis Gyrata Syndrome (BSTVS)

Alias:
Cutis Gyrata Syndrome of Beare and Stevenson
Beare-Stevenson Syndrome
Cutis Gyrata-Acanthosis Nigricans-Craniosynostosis Syndrome
Bstvs
Cutis Gyrata Syndrome of Beare-Stevenson
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Beare-Stevenson Cutis Gyrata Syndrome, also known as cutis gyrata syndrome of beare and stevenson, is related to acanthosis nigricans and hydrocephalus, and has symptoms including respiratory distress An important gene associated with Beare-Stevenson Cutis Gyrata Syndrome is FGFR2 (Fibroblast Growth Factor Receptor 2), and among its related pathways/superpathways are PIP3 activates AKT signaling and Downstream signaling of activated FGFR2. Affiliated tissues include skin and bone, and related phenotypes are ptosis and depressed nasal bridge
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
11
174
11

Medical Symptom

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Description
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No data available

Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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References Literature

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