Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3

Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3: Introduction

Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3: A rare genetic disorder characterized by finger anomalies and premature joining of certain skull bones during development which has an impact on the shape of the head and face. There appears to be considerably variability of symptoms and clinical features of the disorder depending on the exact size and location of the portion of chromosomal material deleted. In this particular form, the chromosomal material deleted is located on chromosome 7 p21.1p21.3. More detailed information about the symptoms, causes, and treatments of Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3 is available below.

Symptoms of Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3

• Premature fusion of skull bones
• Plagiocephaly
• Droopy eyelids
• Webbed fingers
• Learning disability
• more symptoms...»

Read more about symptoms of Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3

Causes of Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3

Read more about causes of Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3.

Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3: Broader Related Topics

• Genetic conditions
• Head conditions
• Musculoskeletal conditions
• Bone or skeletal conditions
• more types...»

Types of Saethre-Chotzen syndrome, chromosome 7 p21.1p21.3

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