Heterozygous otospondylomegaepiphyseal dysplasia

Introduction: Heterozygous otospondylomegaepiphyseal dysplasia

Description of Heterozygous otospondylomegaepiphyseal dysplasia

Heterozygous otospondylomegaepiphyseal dysplasia (medical condition): A very rare inherited disorder involving bone growth abnormalities, impaired hearing and a characteristic face.

See also:

Pierre-Robin syndrome with fetal chondrodysplasia:
  »Introduction: Pierre-Robin syndrome with fetal chondrodysplasia
  »Symptoms of Pierre-Robin syndrome with fetal chondrodysplasia

Heterozygous otospondylomegaepiphyseal dysplasia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Heterozygous otospondylomegaepiphyseal dysplasia:

• Otospondylomegaepiphyseal dysplasia
• Heterozygous
• Dysplasia

Heterozygous otospondylomegaepiphyseal dysplasia as a Disease

Heterozygous otospondylomegaepiphyseal dysplasia: Another name for Pierre-Robin syndrome with fetal chondrodysplasia (or close medical condition association).
  »Introduction: Pierre-Robin syndrome with fetal chondrodysplasia
  »Symptoms of Pierre-Robin syndrome with fetal chondrodysplasia

Symptoms of Heterozygous otospondylomegaepiphyseal dysplasia (Pierre-Robin syndrome with fetal chondrodysplasia)

Some of the symptoms of Heterozygous otospondylomegaepiphyseal dysplasia incude:

• Small jaw
• Rhizomelic chondrodysplasia
• Dumbbell-shaped thigh bone
• Dumbbell-shaped upper arm bone
• Myopia

See full list of 16 symptoms of Heterozygous otospondylomegaepiphyseal dysplasia (Pierre-Robin syndrome with fetal chondrodysplasia)

Heterozygous otospondylomegaepiphyseal dysplasia: Related Disease Topics

These medical disease topics may be related to Heterozygous otospondylomegaepiphyseal dysplasia:

• skeltal abnormalities
• haering loss
• otospondlyomegaepiphyseal dysplasia
• cleft palate
• wide protruding eyes
• dumb-bell shaped bones

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