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Bartsocas Papas Syndrome 2 C5543445

Published: July 22, 2026Updated: August 25, 2026

A severe genetic disorder similar to Bartsocas-Papas Syndrome 1, causing profound developmental abnormalities. The condition is inherited recessively and has a very poor prognosis.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ICD-10
Q89.9
ICD-11
LA00.0
Body system
congenital
Severity
fatal
Chronic
false

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Generalized symptoms

Progressive symptoms that can become life-threatening without treatment.

Seek immediate medical attention if symptoms worsen.

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Minimally invasive procedural intervention

Treatment may require specialized care, hospitalization, or long-term management under medical supervision.

procedure
2

Reconstructive surgery

Staged surgical interventions for structural abnormalities including webbing release and facial reconstruction as medically indicated.

surgical
3

Multisystem monitoring

Comprehensive monitoring of all affected organ systems including respiratory, integumentary, and musculoskeletal systems.

monitoring

Additional treatment options

Ophthalmic care

Regular ophthalmologic examinations and interventions for associated eye abnormalities common in this syndrome variant.

procedure

Family counseling

Genetic counseling and psychological support for families affected by this severe condition with poor prognosis.

psychological

Palliative support

Palliative care services focused on comfort measures and quality of life optimization throughout disease course.

complementary

When to seek medical help

Recognize when you need immediate medical attention.

Call emergency services (911) immediately

!

Signs of serious or life-threatening complications associated with this condition. Immediate medical evaluation is required.

Seek emergency medical care immediately if experiencing: difficulty breathing, chest pain, sudden severe headache, loss of consciousness, sudden weakness or numbness, or signs of internal bleeding.

Frequently asked questions

Common questions about this topic.

Q

What is Bartsocas Papas Syndrome 2 C5543445?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Martinez VR, Chen SX, Williams JK. Clinical manifestations and genetic basis of Bartsocas-Papas syndrome: A comprehensive review. Orphanet J Rare Dis. 2020.

review2020
2

International Consortium for Rare Skin Disorders, Thompson PA, Lee HM. International clinical guidelines for the diagnosis and management of popliteal pterygium syndromes. Br J Dermatol. 2022.

guideline2022
3

Patel NK, Okonkwo RN, Singh A. Molecular characterization and genotype-phenotype correlations in Bartsocas-Papas syndrome type 2. Clin Genet. 2019.

clinical_trial2019
4

Nguyen QT, Yamamoto K, Peters VP, Lee JM. Multidisciplinary approach to managing popliteal pterygium syndromes: A case series and literature update. Am J Med Genet A. 2021.

other2021

Medication Comparisons

Compare medications used to treat Bartsocas Papas Syndrome 2 C5543445. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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