How to Check the Marfan Syndrome Thumb & Wrist Signs
At a Glance
The thumb (Steinberg) and wrist (Walker-Murdoch) signs test for long fingers and loose joints, which are common in Marfan syndrome. However, testing positive does not mean you have the condition. A doctor must evaluate your heart and eyes for a true Marfan syndrome diagnosis.
When evaluating for Marfan syndrome, doctors often check for two physical indicators known as the Steinberg (thumb) sign and the Walker-Murdoch (wrist) sign. These are quick, simple physical tests that help identify if a person has unusually long, slender fingers and loose joints [1][2]. While these tests are iconic features of Marfan syndrome, testing positive for one or both does not automatically mean you have the condition [3].
The Steinberg (Thumb) Sign
The Steinberg sign evaluates finger length and joint flexibility.
- How to check: Hold your hand out flat. Fold your thumb across your palm, and then close your other four fingers over the thumb to make a fist.
- A positive sign: The test is positive if the entire tip of your thumb (distal phalanx), including the thumbnail, sticks out visibly beyond the far edge (the pinky side) of your palm [4].
The Walker-Murdoch (Wrist) Sign
The Walker-Murdoch sign also checks for long bones and joint flexibility, specifically in the wrist and fingers.
- How to check: Use your thumb and pinky (little finger) to wrap around the narrowest part of your opposite wrist.
- A positive sign: The test is positive if the tips of your thumb and pinky overlap each other while gripping the wrist [4].
What Do These Signs Indicate?
If you have a positive thumb or wrist sign, it usually points to a combination of two physical traits [1]:
- Arachnodactyly (long bone overgrowth): A medical term that means fingers are disproportionately long and slender compared to the rest of the hand or body [5].
- Joint hypermobility: Often called “loose joints,” this means the ligaments that hold your joints together are more relaxed, allowing the joints to stretch further than usual [1]. Children naturally have looser joints, so false positives can be particularly common in youth.
Because Marfan syndrome is a disorder of the body’s connective tissue, people with the condition frequently display both of these traits [2].
Why Positive Signs Don’t Mean a Diagnosis
It is crucial to understand that having a positive thumb or wrist sign does not mean you have Marfan syndrome [1][3]. These physical features can be found in people with other connective tissue conditions (such as Ehlers-Danlos syndrome), in people with a naturally slender build, or in people who just happen to be double-jointed [1][3]. Conversely, it is entirely possible to have Marfan syndrome even if you do not display these specific signs.
Doctors use a checklist called the Revised Ghent Nosology to diagnose Marfan syndrome [6][4]. In this scoring system:
- Having only one of the signs gives you 1 point.
- Having both a positive thumb and wrist sign gives you 3 points [4].
- A score of 7 or higher is needed just to meet the “systemic” (whole body) criteria for the condition [4].
A definitive diagnosis relies heavily on more significant signs that cannot be seen on the outside of the body, particularly an enlarged aorta (aortic root aneurysm) or a dislocated lens in the eye (ectopia lentis) [4]. If you notice these thumb and wrist signs in yourself or a family member, it is simply a piece of information to discuss with your doctor rather than a reason to panic.
Common questions in this guide
How do you do the thumb test (Steinberg sign) for Marfan syndrome?
What is the wrist test (Walker-Murdoch sign) for Marfan syndrome?
If my thumb or wrist test is positive, do I have Marfan syndrome?
What does arachnodactyly mean?
Questions to Ask Your Doctor
Curated prompts to bring to your next appointment.
- 1.Could my joint flexibility and finger length be related to a connective tissue disorder, or are they just my natural build?
- 2.Do you recommend I have an echocardiogram to check my aorta or see an eye doctor to look for lens dislocation?
- 3.Should I be referred to a medical geneticist for a formal evaluation using the Ghent criteria?
- 4.Are there other systemic signs of Marfan syndrome that you observe during my physical exam?
Questions For You
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References
References (6)
- 1
Hyperdynamic Valve: A Rare Case of Ehlers-Danlos Syndrome.
Pires SX, Pereira G, Paiva D, et al.
Journal of medical cases 2021; (12(7)):284-287 doi:10.14740/jmc3692.
PMID: 34434473 - 2
Evaluation of the clinical features of an outpatient cohort with Marfan syndrome.
Ribeiro WN, Leite WF, Vallim ALVA, et al.
International journal of cardiology 2025; (418()):132604 doi:10.1016/j.ijcard.2024.132604.
PMID: 39366558 - 3
Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndrome.
Oba D, Sagara M, Oda S, et al.
Human genome variation 2025; (12(1)):24 doi:10.1038/s41439-025-00329-9.
PMID: 41145435 - 4
The revised Ghent nosology for the Marfan syndrome.
Loeys BL, Dietz HC, Braverman AC, et al.
Journal of medical genetics 2010; (47(7)):476-85 doi:10.1136/jmg.2009.072785.
PMID: 20591885 - 5
Orthopaedic Aspects of Marfan Syndrome: The Experience of a Referral Center for Diagnosis of Rare Diseases.
De Maio F, Fichera A, De Luna V, et al.
Advances in orthopedics 2016; (2016()):8275391 doi:10.1155/2016/8275391.
PMID: 28050285 - 6
Predictive Physical Manifestations for Progression of Scoliosis in Marfan Syndrome.
Taniguchi Y, Matsubayashi Y, Kato S, et al.
Spine 2021; (46(15)):1020-1025 doi:10.1097/BRS.0000000000003939.
PMID: 34228694
This page explains physical signs sometimes associated with Marfan syndrome for educational purposes only. Only a qualified healthcare provider or medical geneticist can diagnose a connective tissue disorder.
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