Metaphyseal dysplasia: Difference between revisions

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'''Metaphyseal dysplasia''' is a rare genetic disorder that affects the metaphyses of the bones. The metaphyses are the wide portions at the ends of the long bones, such as the femur and humerus, where growth occurs in children. In individuals with metaphyseal dysplasia, these areas are malformed, leading to a variety of skeletal abnormalities.
{{SI}}
 
{{Infobox medical condition
==Symptoms==
| name            = Metaphyseal dysplasia
The symptoms of metaphyseal dysplasia can vary greatly from person to person. Some individuals may have mild symptoms, while others may have severe skeletal abnormalities. Common symptoms include:
| image          = [[File:Autosomal_recessive_-_en.svg|200px]]
 
| caption        = Metaphyseal dysplasia is often inherited in an [[autosomal recessive]] pattern.
* Short stature
| synonyms        = Pyle disease
* Bowing of the legs
| specialty      = [[Medical genetics]], [[Orthopedics]]
* Abnormal curvature of the spine ([[scoliosis]])
| symptoms        = [[Bone deformities]], [[joint pain]], [[short stature]]
* Joint pain and stiffness
| onset          = Childhood
* Limited range of motion in the joints
| duration        = Lifelong
 
| causes          = Genetic mutations
==Causes==
| risks          = Family history
Metaphyseal dysplasia is caused by mutations in certain genes that are involved in the development and growth of bone. These mutations are usually inherited in an autosomal dominant manner, which means that an affected individual has a 50% chance of passing the disorder on to each of their children.
| diagnosis      = [[Radiography]], [[Genetic testing]]
 
| differential    = [[Osteopetrosis]], [[Rickets]]
==Diagnosis==
| treatment      = [[Physical therapy]], [[Orthopedic surgery]]
The diagnosis of metaphyseal dysplasia is usually made based on the clinical symptoms and physical examination findings. Imaging studies, such as X-rays, can also be helpful in confirming the diagnosis. In some cases, genetic testing may be used to identify the specific gene mutation causing the disorder.
| prognosis      = Variable, generally good with management
 
| frequency      = Rare
==Treatment==
}}
There is currently no cure for metaphyseal dysplasia. Treatment is aimed at managing the symptoms and improving the quality of life for individuals with the disorder. This may include physical therapy, pain management, and in some cases, orthopedic surgery to correct skeletal abnormalities.
'''Metaphyseal dysplasia''', also known as Pyle's disease, is a rare genetic disorder that affects the [[metaphysis]] of the [[long bones]]. It is characterized by abnormal bone development, particularly in the metaphyseal regions, leading to a range of skeletal abnormalities.
 
=== Etiology ===
==See also==
Metaphyseal dysplasia is primarily inherited in an [[autosomal recessive]] pattern, meaning that an individual must inherit two copies of the defective gene, one from each parent, to manifest the disease. The specific genetic mutations responsible for this condition are not fully understood, but they result in defective bone remodeling and growth.
* [[Genetic disorders]]
=== Clinical Features ===
* [[Bone diseases]]
Patients with metaphyseal dysplasia typically present with:
* [[Growth disorders]]
* Widening of the metaphyses of long bones, particularly in the [[femur]] and [[tibia]].
 
* Bowing of the legs, which may lead to [[genu varum]] or [[genu valgum]].
==References==
* Short stature due to impaired growth of the long bones.
<references />
* Increased risk of [[fractures]] due to bone fragility.
 
=== Diagnosis ===
Diagnosis of metaphyseal dysplasia is based on clinical evaluation, family history, and radiographic findings. X-rays typically show:
* Widened metaphyses with a "Erlenmeyer flask" appearance.
* Cortical thinning and reduced bone density.
=== Management ===
There is no cure for metaphyseal dysplasia, and treatment is primarily supportive. Management strategies include:
* Orthopedic interventions to correct bone deformities and improve function.
* Physical therapy to enhance mobility and strength.
* Monitoring for potential complications such as fractures.
=== Prognosis ===
The prognosis for individuals with metaphyseal dysplasia varies depending on the severity of the condition. While the disorder can lead to significant skeletal deformities, many individuals can lead relatively normal lives with appropriate management.
== See Also ==
* [[Osteogenesis imperfecta]]
* [[Achondroplasia]]
* [[Skeletal dysplasia]]
{{Skeletal disorders}}
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Bone diseases]]
[[Category:Orthopedic conditions]]
[[Category:Growth disorders]]
 
{{stub}}

Latest revision as of 05:09, 6 April 2025

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

Metaphyseal dysplasia
Synonyms Pyle disease
Pronounce N/A
Specialty Medical genetics, Orthopedics
Symptoms Bone deformities, joint pain, short stature
Complications N/A
Onset Childhood
Duration Lifelong
Types N/A
Causes Genetic mutations
Risks Family history
Diagnosis Radiography, Genetic testing
Differential diagnosis Osteopetrosis, Rickets
Prevention N/A
Treatment Physical therapy, Orthopedic surgery
Medication N/A
Prognosis Variable, generally good with management
Frequency Rare
Deaths N/A


Metaphyseal dysplasia, also known as Pyle's disease, is a rare genetic disorder that affects the metaphysis of the long bones. It is characterized by abnormal bone development, particularly in the metaphyseal regions, leading to a range of skeletal abnormalities.

Etiology[edit]

Metaphyseal dysplasia is primarily inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the defective gene, one from each parent, to manifest the disease. The specific genetic mutations responsible for this condition are not fully understood, but they result in defective bone remodeling and growth.

Clinical Features[edit]

Patients with metaphyseal dysplasia typically present with:

  • Widening of the metaphyses of long bones, particularly in the femur and tibia.
  • Bowing of the legs, which may lead to genu varum or genu valgum.
  • Short stature due to impaired growth of the long bones.
  • Increased risk of fractures due to bone fragility.

Diagnosis[edit]

Diagnosis of metaphyseal dysplasia is based on clinical evaluation, family history, and radiographic findings. X-rays typically show:

  • Widened metaphyses with a "Erlenmeyer flask" appearance.
  • Cortical thinning and reduced bone density.

Management[edit]

There is no cure for metaphyseal dysplasia, and treatment is primarily supportive. Management strategies include:

  • Orthopedic interventions to correct bone deformities and improve function.
  • Physical therapy to enhance mobility and strength.
  • Monitoring for potential complications such as fractures.

Prognosis[edit]

The prognosis for individuals with metaphyseal dysplasia varies depending on the severity of the condition. While the disorder can lead to significant skeletal deformities, many individuals can lead relatively normal lives with appropriate management.

See Also[edit]