Spondyloepimetaphyseal dysplasia

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Spondyloepimetaphyseal dysplasia
Synonyms	N/A
Pronounce	N/A
Specialty	N/A
Symptoms	Short stature, abnormal curvature of the spine, joint pain
Complications	Arthritis, scoliosis, kyphosis
Onset	Childhood
Duration	Lifelong
Types	Strudwick type, Missouri type, Pakistani type
Causes	Genetic mutations
Risks	Family history
Diagnosis	Genetic testing, X-ray
Differential diagnosis	Achondroplasia, Metaphyseal dysplasia
Prevention	N/A
Treatment	Physical therapy, orthopedic surgery
Medication	Pain management
Prognosis	Varies depending on type and severity
Frequency	Rare
Deaths	N/A

Spondyloepimetaphyseal dysplasia (SEMD) is a group of rare genetic disorders that affect bone growth, particularly in the spine (vertebrae), the ends of long bones (epiphyses), and the bones of the hands and feet (metaphyses). These conditions are part of a larger group of disorders known as skeletal dysplasias, which are characterized by abnormalities in the size and shape of the limbs, trunk, and skull.

Causes

SEMD is caused by mutations in various genes that are important for the development and maintenance of bone and cartilage. These mutations are usually inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected. In some cases, SEMD can be inherited in an autosomal dominant pattern, where only one copy of the mutated gene is sufficient to cause the disorder.

Symptoms

The symptoms of SEMD can vary widely among affected individuals but generally include:

• Short stature, often with a short trunk
• Abnormal curvature of the spine (Scoliosis and/or Kyphosis)
• Abnormalities in the shape of the vertebrae
• Flattened bones at the ends of the long bones (epiphyses)
• Abnormal bone growth in the hands and feet

Other possible features include problems with vision and hearing, joint stiffness, and difficulties with mobility.

Diagnosis

Diagnosis of SEMD typically involves a combination of clinical examination, family history, and imaging studies such as X-rays, which can reveal characteristic abnormalities in bone structure. Genetic testing may also be performed to identify specific mutations causing the disorder.

Treatment

There is no cure for SEMD, but treatment is focused on managing symptoms and improving quality of life. This may include:

• Physical therapy to improve mobility and strength
• Orthopedic interventions, such as surgery, to correct bone deformities and improve function
• Pain management strategies
• Regular monitoring for potential complications, such as breathing difficulties due to chest wall deformities

Prognosis

The prognosis for individuals with SEMD varies depending on the severity of the symptoms and the specific genetic cause. While some individuals may experience significant physical limitations, others may lead relatively normal lives with appropriate management and support.

See also

• Osteochondrodysplasia
• Achondroplasia
• Marfan syndrome
• Ehlers-Danlos syndrome

   This article is a medical stub. You can help WikiMD by expanding it!