Chondrodystrophia punctata, autosomal dominant

Chondrodystrophia punctata, autosomal dominant: Introduction

Chondrodystrophia punctata, autosomal dominant: A rare genetic disorder characterized by growth deficiency, short limbs, large skin pores, sparse hair and other abnormalities. More detailed information about the symptoms, causes, and treatments of Chondrodystrophia punctata, autosomal dominant is available below.

Symptoms of Chondrodystrophia punctata, autosomal dominant

• Growth deficiency
• Low nose bridge
• Flat face
• Underdeveloped cheeks
• Down-slanting eye slits
• more symptoms...»

See full list of 18 symptoms of Chondrodystrophia punctata, autosomal dominant

Chondrodystrophia punctata, autosomal dominant: Complications

Review possible medical complications related to Chondrodystrophia punctata, autosomal dominant:

• Orthopedic problems
• Infant death
• Stillbirth
• more complications...»

Less Common Symptoms of Chondrodystrophia punctata, autosomal dominant

• Abnormal ears
• Minor nail anomalies
• Nystagmus
• Hazy cornea
• Small eyes
• more symptoms...»

See full list of 21 occasional symptoms of Chondrodystrophia punctata, autosomal dominant

Wrongly Diagnosed with Chondrodystrophia punctata, autosomal dominant?

• Failure to diagnose Chondrodystrophia punctata, autosomal dominant
• Undiagnosed: Chondrodystrophia punctata, autosomal dominant

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• What is Chondrodystrophia punctata, autosomal dominant?
• Symptoms of Chondrodystrophia punctata, autosomal dominant
• Signs of Chondrodystrophia punctata, autosomal dominant
• Complications of Chondrodystrophia punctata, autosomal dominant
• Undiagnosed Chondrodystrophia punctata, autosomal dominant

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