Schöpf - Schulz - Passarge - Syndrome
Last Updated: 2023-07-07
Author(s): Anzengruber F., Navarini A.
ICD11: -
Last Updated: 2023-07-07
Author(s): Anzengruber F., Navarini A.
ICD11: -
Schöpf et al. 1971
Palmoplantar keratosis, which is caused by a mutation in the WNT10A gene. In addition to the cutaneous manifestations, hypodonia and hypotrichosis are characteristic. Eyelid cysts are also present in most patients.
Autosomal – recessive mutation of the WNT10A gene.
Palmoplantar keratosis.
Hypotrichia.
Hypodentia.
Lid cysts.
Anamnesis.
Clinical.
Genetic analysis.
Dental consultation.
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