Chromosome 10p duplication/10q deletion syndrome

Chromosome 10p duplication/10q deletion syndrome: Introduction

Chromosome 10p duplication/10q deletion syndrome: A rare chromosomal disorder where a section of the short arm (p) of chromosome 10 is duplicated and a section of the long arm (q) of chromosome 10 is deleted resulting in various abnormalities. More detailed information about the symptoms, causes, and treatments of Chromosome 10p duplication/10q deletion syndrome is available below.

Symptoms of Chromosome 10p duplication/10q deletion syndrome

• Small head
• Long head
• Flat back of skull
• Retrognathia
• Small jaw
• more symptoms...»

See full list of 37 symptoms of Chromosome 10p duplication/10q deletion syndrome

Wrongly Diagnosed with Chromosome 10p duplication/10q deletion syndrome?

• Failure to diagnose Chromosome 10p duplication/10q deletion syndrome
• Undiagnosed: Chromosome 10p duplication/10q deletion syndrome

Chromosome 10p duplication/10q deletion syndrome: Complications

Review possible medical complications related to Chromosome 10p duplication/10q deletion syndrome:

• Infant death #most die during first year
• more complications...»

Causes of Chromosome 10p duplication/10q deletion syndrome

Read more about causes of Chromosome 10p duplication/10q deletion syndrome.

Disease Topics Related To Chromosome 10p duplication/10q deletion syndrome

Research the causes of these diseases that are similar to, or related to, Chromosome 10p duplication/10q deletion syndrome:

• Hypotonia
• Poor feeding
• Mental retardation
• Cranial anomalies
• Microcephaly
• Dolichocephaly
• more related diseases...»

Chromosome 10p duplication/10q deletion syndrome: Broader Related Topics

• Genetic conditions
• more types...»

Types of Chromosome 10p duplication/10q deletion syndrome

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Definitions of Chromosome 10p duplication/10q deletion syndrome:

Duplication of a portion of the short arm of chromosome 10 combined with deletion of the long arm of chromosome 10. Clinical manifestations are similar to those seen in patients with chromosome 10p duplication and chromosome 10q deletion syndromes. The most frequently occurring defects include central nervous system disorders (hypotonia, poor feeding, and mental retardation), cranial anomalies (microcephaly, dolichocephaly, retrognathia, wide sutures, frontal bossing, cleft lip and palate, and nose malformations), skeletal deformities (clinodactyly, camptodactyly, and clubfoot), urogenital anomalies, and cardiac defects. - (Source - Diseases Database)

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