Idiopathic camptocormia

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ORPHA:1320M43.8
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1Active trials2Specialists8Treatment centers

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UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Idiopathic camptocormia, also known as idiopathic bent spine syndrome, is a rare postural disorder characterized by an abnormal, involuntary forward flexion of the thoracolumbar spine that appears during standing or walking and disappears in the supine (lying down) position. The term 'camptocormia' derives from the Greek words 'kamptos' (to bend) and 'kormos' (trunk). In the idiopathic form, no identifiable underlying neurological, muscular, or skeletal cause can be found, distinguishing it from secondary camptocormia which may occur in the context of Parkinson's disease, myopathies, dystonia, or other conditions. The condition primarily affects the musculoskeletal system, specifically the paraspinal (back extensor) muscles. Patients typically present with a forward trunk flexion of 45 degrees or more that worsens with prolonged standing or walking and is fully reducible when lying flat or when the patient leans against a wall. This abnormal posture can lead to significant functional impairment, back pain, fatigue, difficulty with balance, and reduced quality of life. Some patients may also experience difficulty breathing due to the compressed thoracic cavity. Imaging of the paraspinal muscles may reveal fatty infiltration and atrophy, though the cause of these changes remains unclear in the idiopathic form. Treatment of idiopathic camptocormia is largely supportive and symptomatic. Physical therapy and rehabilitation programs focusing on strengthening the trunk extensor muscles and improving posture are considered first-line approaches. Orthotic devices such as thoracolumbar braces or corsets may provide temporary relief. In refractory cases, spinal surgery with instrumented fusion has been attempted, though outcomes are variable and complications can occur. There is no established pharmacological treatment specifically for the idiopathic form, and the condition tends to be chronic and progressive in many patients.

Also known as:

Clinical phenotype terms— hover any for plain English:

EMG: neuropathic changesHP:0003445Abnormal intervertebral disk morphologyHP:0005108EMG: impaired neuromuscular transmissionHP:0100285Abnormality of the headHP:0000234Proximal spinal muscular atrophyHP:0006959Amyotrophic lateral sclerosisHP:0007354Abnormal inflammatory responseHP:0012647Abnormal basal ganglia morphologyHP:0002134Frontotemporal dementiaHP:0002145
Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Late onset

Begins later in life, typically after age 50

Orphanet ↗NORD ↗

FDA & Trial Timeline

2 events
Aug 2025Evaluation of the Safety of Electrical Spinal Cord Stimulation in Parkinson's Patients Presenting With Painful Camptocormia

University Hospital, Rouen — NA

TrialRECRUITING
Aug 2021The Effect of Spinal Mobilization on Respiratory Parameters in Parkinson's Disease Patients

Abant Izzet Baysal University — NA

TrialRECRUITING

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

No FDA-approved treatments are currently listed for Idiopathic camptocormia.

1 clinical trialare actively recruiting — trials can provide access to cutting-edge therapies.

View clinical trials →

Clinical Trials

1 recruitingView all trials with filters →
N/A1 trial
The Effect of Spinal Mobilization on Respiratory Parameters in Parkinson's Disease Patients
N/A
Actively Recruiting
PI: Ramazan Kurul, Ph.D (Abant Izzet Baysal University) · Sites: Bolu; Bolu · Age: 5085 yrs

Specialists

2 foundView all specialists →
RP
Ramazan Kurul, Ph.D
Specialist
PI on 1 active trial
VS
Vincenzo Maria Saraceni
Specialist
PI on 2 active trials16 Idiopathic camptocormia publications

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Idiopathic camptocormia.

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Community

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Latest news about Idiopathic camptocormia

Disease timeline:

New recruiting trial: Evaluation of the Safety of Electrical Spinal Cord Stimulation in Parkinson's Patients Presenting With Painful Camptocormia

A new clinical trial is recruiting patients for Idiopathic camptocormia

New recruiting trial: The Effect of Spinal Mobilization on Respiratory Parameters in Parkinson's Disease Patients

A new clinical trial is recruiting patients for Idiopathic camptocormia

Caregiver Resources

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Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about Idiopathic camptocormia

What is Idiopathic camptocormia?

Idiopathic camptocormia, also known as idiopathic bent spine syndrome, is a rare postural disorder characterized by an abnormal, involuntary forward flexion of the thoracolumbar spine that appears during standing or walking and disappears in the supine (lying down) position. The term 'camptocormia' derives from the Greek words 'kamptos' (to bend) and 'kormos' (trunk). In the idiopathic form, no identifiable underlying neurological, muscular, or skeletal cause can be found, distinguishing it from secondary camptocormia which may occur in the context of Parkinson's disease, myopathies, dystonia,

How is Idiopathic camptocormia inherited?

Idiopathic camptocormia follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Idiopathic camptocormia typically begin?

Typical onset of Idiopathic camptocormia is late onset. Age of onset can vary across affected individuals.

Are there clinical trials for Idiopathic camptocormia?

Yes — 1 recruiting clinical trial is currently listed for Idiopathic camptocormia on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.

Which specialists treat Idiopathic camptocormia?

2 specialists and care centers treating Idiopathic camptocormia are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.