Cranioectodermal Dysplasia 2 C3150874
A genetic condition similar to CED1, involving abnormalities in bones, skin, hair, and teeth. Managed by a team of specialists addressing the various manifestations throughout life.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Short stature
(musculoskeletal)Sparse hair
(integumentary)Skeletal dysplasia
(musculoskeletal)Hypodontia
(dental)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Drug therapy and clinical monitoring
Active treatment with regular monitoring by a healthcare provider is recommended.
Comprehensive medical surveillance
Regular monitoring for organ involvement including hepatic, renal, and cardiac assessments typical of this subtype, with periodic imaging and laboratory evaluation to detect complications early.
Orthopedic intervention program
Surgical management of skeletal manifestations including surgical correction of limb abnormalities, joint deformities, and spinal curvature when conservative measures fail to provide adequate function.
Additional treatment options
Psychosocial support services
Mental health support including counseling and support groups to address the psychosocial impact of living with a rare genetic condition affecting appearance and physical function.
psychologicalAdaptive lifestyle modifications
Environmental adaptations and assistive devices to maximize independence and safety, including home modifications, mobility aids, and adaptive equipment for daily activities.
lifestyleFunctional mobility therapy
Ongoing physical therapy focusing on maintaining joint range of motion, muscle strength, and functional mobility appropriate to the individual's skeletal abnormalities and overall health status.
physical_therapyWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Cranioectodermal Dysplasia 2 C3150874?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalMedication Comparisons
Compare medications used to treat Cranioectodermal Dysplasia 2 C3150874. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy