Chromosome 10p deletion syndrome (medical condition): A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 10 resulting in variable abnormalities.
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Chromosome 10p deletion syndrome:
»Introduction: Chromosome 10p deletion syndrome
»Symptoms of Chromosome 10p deletion syndrome
»Treatments for Chromosome 10p deletion syndrome
Chromosome 10p deletion syndrome: Deletion of the short arm of chromosome 10 with retarded psychomotor development and variable abnormalities, including dwarfism, craniofacial dysmorphism (downslanting palpebral fissures, anteverted nostrils, and eye and ear anomalies), deformed hands and feet, cryptorchidism, and dysplasia of the olfactory system.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Chromosome 10p deletion syndrome:
Chromosome 10p deletion syndrome (medical condition): See Chromosome 10p deletion syndrome (disease information).
»Introduction: Chromosome 10p deletion syndrome
»Symptoms of Chromosome 10p deletion syndrome
»Treatments for Chromosome 10p deletion syndrome
These medical disease topics may be related to Chromosome 10p deletion syndrome:
Source: Diseases Database
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