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Medical Genetics

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?
Hold your hand flat, fold your thumb across your palm, and close your other fingers over it to make a fist. The test is considered positive if the entire tip of your thumb sticks out visibly beyond the pinky side of your hand.
What is the wrist test (Walker-Murdoch sign) for Marfan syndrome?
Use your thumb and pinky finger to wrap around the narrowest part of your opposite wrist. If the tips of your thumb and pinky overlap each other while gripping the wrist, it is a positive sign.
If my thumb or wrist test is positive, do I have Marfan syndrome?
Not necessarily. Many people without Marfan syndrome have a slender build or flexible joints. Doctors use these signs as just one part of a larger scoring system, called the Ghent criteria, to determine if you need further evaluation.
What does arachnodactyly mean?
Arachnodactyly is a medical term that describes fingers and toes that are disproportionately long and slender compared to the rest of the body. It is one of the physical traits checked for during the thumb and wrist tests.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Could my joint flexibility and finger length be related to a connective tissue disorder, or are they just my natural build?
  2. 2.Do you recommend I have an echocardiogram to check my aorta or see an eye doctor to look for lens dislocation?
  3. 3.Should I be referred to a medical geneticist for a formal evaluation using the Ghent criteria?
  4. 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. 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. 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. 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. 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. 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. 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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