Conditions / Syndrome
dyschromatosis, ichthyosis, deafness, and atopic disease
info · Syndrome
A syndrome characterized by generalized hyperpigmentation with hypopigmented spots, ichthyosis, sensorineural hearing loss, atopic dermatitis, asthma, and allergic rhinitis that has_material_basis_in compound heterozygous mutation in the OSBPL2 gene on chromos
A syndrome characterized by generalized hyperpigmentation with hypopigmented spots, ichthyosis, sensorineural hearing loss, atopic dermatitis, asthma, and allergic rhinitis that has_material_basis_in compound heterozygous mutation in the OSBPL2 gene on chromosome 20q13.
Signs and symptoms
- Chronic rhinitis
- Hypopigmented macule
- Asthma
- Facial telangiectasia
- Ichthyosis
- Sensorineural hearing impairment
- Generalized hyperpigmentation
- Eczematoid dermatitis
- Hyperkeratosis
- Atopic dermatitis
Also known as: DIDA