Metaphyseal dysplasia: Difference between revisions

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== Metaphyseal Dysplasia ==
{{SI}}
 
{{Infobox medical condition
[[File:Autosomal_recessive_-_en.svg|thumb|right|Diagram illustrating autosomal recessive inheritance.]]
| name            = Metaphyseal dysplasia
 
| image          = [[File:Autosomal_recessive_-_en.svg|200px]]
| caption        = Metaphyseal dysplasia is often inherited in an [[autosomal recessive]] pattern.
| synonyms        = Pyle disease
| specialty      = [[Medical genetics]], [[Orthopedics]]
| symptoms        = [[Bone deformities]], [[joint pain]], [[short stature]]
| onset          = Childhood
| duration        = Lifelong
| causes          = Genetic mutations
| risks          = Family history
| diagnosis      = [[Radiography]], [[Genetic testing]]
| differential    = [[Osteopetrosis]], [[Rickets]]
| treatment      = [[Physical therapy]], [[Orthopedic surgery]]
| prognosis      = Variable, generally good with management
| frequency      = Rare
}}
'''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.
'''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 ===
=== Etiology ===
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.
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 ===
=== Clinical Features ===
Patients with metaphyseal dysplasia typically present with:
Patients with metaphyseal dysplasia typically present with:
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* Short stature due to impaired growth of the long bones.
* Short stature due to impaired growth of the long bones.
* Increased risk of [[fractures]] due to bone fragility.
* Increased risk of [[fractures]] due to bone fragility.
=== Diagnosis ===
=== Diagnosis ===
Diagnosis of metaphyseal dysplasia is based on clinical evaluation, family history, and radiographic findings. X-rays typically show:
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.
* Widened metaphyses with a "Erlenmeyer flask" appearance.
* Cortical thinning and reduced bone density.
* Cortical thinning and reduced bone density.
=== Management ===
=== Management ===
There is no cure for metaphyseal dysplasia, and treatment is primarily supportive. Management strategies include:
There is no cure for metaphyseal dysplasia, and treatment is primarily supportive. Management strategies include:
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* Physical therapy to enhance mobility and strength.
* Physical therapy to enhance mobility and strength.
* Monitoring for potential complications such as fractures.
* Monitoring for potential complications such as fractures.
=== Prognosis ===
=== 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.
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 ==
== Related Pages ==
* [[Osteogenesis imperfecta]]
* [[Osteogenesis imperfecta]]
* [[Achondroplasia]]
* [[Achondroplasia]]
* [[Skeletal dysplasia]]
* [[Skeletal dysplasia]]
{{Skeletal disorders}}
{{Skeletal disorders}}
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Orthopedic conditions]]
[[Category:Orthopedic conditions]]

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]