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camptodactyly

vr.tr.camptodactyly · thing-q614013

Enable an agent to recognise camptodactyly, record finger-specific severity and progression, and support clinician-led decisions about observation, therapy and specialist assessment.

Thing Registry Cross-cutting context XCT.STA

Bundle → Layer → Finding → Questions Filled

5 bundles · 9 layers · 14 findings · 28 questions

Phenotype and diagnostic boundaries Establish which finger posture is being modelled and why it is considered camptodactyly.

Joint pattern

Localise the deformity and distinguish active limitation from fixed restriction.

PIP flexion phenotype

Camptodactyly typically involves incomplete PIP extension; some affected joints remain passively correctable. [Boston Children's Hospital](https://www.childrenshospital.org/sites/default/files/2022-04/camptodactyly-factsheet.pdf)

  1. Which fingers and joints show persistent flexion, and on which hand? measurement
  2. Can each affected PIP joint straighten actively, passively, both or neither? measurement

Alternative explanations

Check whether a different deformity or acquired process better explains the finding.

Diagnostic attribution

Keep the observed posture separate from the clinician's diagnostic interpretation.

  1. Is the principal abnormality PIP flexion, sideways angulation, or a different joint pattern? boundary
  2. What history or examination evidence supports an alternative involving injury, scarring, inflammation or triggering? boundary
  3. Who established the diagnosis, when, and what uncertainty remains? provenance
Presentation and associations Record developmental timing and evidence for a broader phenotype.

Developmental history

Separate onset, recognition and subsequent growth-related change.

Onset evidence

Use dated observations rather than inferring congenital onset from the diagnostic label.

  1. When was the bend first observed, and is there evidence of an earlier normal or abnormal posture? provenance
  2. Did the finger posture change during a documented period of rapid growth? measurement

Familial and systemic context

Link relevant family history and additional findings without assigning an unsupported cause.

Isolated or associated presentation

Family history or a wider syndrome may accompany camptodactyly; either association needs its own evidence. [Boston Children's Hospital](https://www.childrenshospital.org/sites/default/files/2022-04/camptodactyly-factsheet.pdf)

  1. Which relatives have a comparable finger phenotype, and was it examined or only reported? provenance
  2. What additional contractures or extra-hand findings support assessment for an associated syndrome? boundary
  3. Is a syndrome confirmed, suspected or unassessed, and which separate model should own it? boundary
Severity and course Connect comparable joint measurements with actual consequences for hand use.

Motion and change

Measure extension and retained flexion for each affected digit over time.

Comparable motion record

Document measurement conditions so apparent progression can be distinguished from examination variation.

  1. What are the active and passive PIP extension deficits and available flexion, in degrees? measurement
  2. Were wrist position, adjacent-joint position and measurement method comparable with the previous assessment? measurement
  3. What observed change supports stable, worsening, improving or recurrent status? measurement

Functional and symptom burden

Capture task limitations, appearance concerns and symptoms that need separate explanation.

Patient-important effects

Camptodactyly may have little pain or functional effect; record individual burden rather than assuming disability from appearance. [Children's Hospital of Philadelphia](https://www.chop.edu/conditions-diseases/camptodactyly)

  1. Which tasks are affected, such as gripping, releasing objects, writing or putting on gloves? measurement
  2. What matters most to the person: function, appearance, comfort or preventing further change? action
  3. Are pain, swelling, warmth or sensory symptoms present, and do they require investigation beyond the contracture? boundary
Management and outcomes Support review of clinician-directed care and its effects on useful finger movement.

Care selection and delivery

Record the reason for observation, therapy or specialist intervention and what care was delivered.

Individualised care plan

Care can include stretching, splinting or surgery, with selection informed by severity and function. [Children's Hospital of Philadelphia](https://www.chop.edu/conditions-diseases/camptodactyly)

  1. What findings and goals justify the clinician's current choice of observation, therapy or surgical assessment? action
  2. What stretching or splint programme was prescribed, and what was actually completed and tolerated? provenance
  3. What change should prompt an earlier review, and who is responsible for follow-up? action

Benefit and residual limitation

Evaluate extension gains alongside flexion, function and durability.

Balanced treatment outcome

Residual curvature and stiffness can remain after surgery, so outcome assessment must include retained movement. [Boston Children's Hospital](https://www.childrenshospital.org/sites/default/files/2022-04/camptodactyly-factsheet.pdf)

  1. How did active extension, passive extension, flexion and priority tasks change from the pretreatment baseline? measurement
  2. Is there residual or recurrent contracture, new stiffness, pain or difficulty using the finger? measurement
  3. Does the observed benefit justify continuing or revising the plan at clinician review? action
Evidence and external alignment What the world already says about this thing, gathered so the model can be checked against it.

Reported evidence

Findings from the breadth pass, kept separate from the structural claims.

Check these first

Recalled without web access and unsourced; every item is a lead to verify.

  1. Which of these check these first hold for the sense of camptodactyly this model covers, and on what evidence? provenance

Kinds and varieties

Recalled without web access and unsourced; every item is a lead to verify.

  1. Which of these kinds and varieties hold for the sense of camptodactyly this model covers, and on what evidence? provenance

Real-world use

Recalled without web access and unsourced; every item is a lead to verify.

  1. Which of these real-world use hold for the sense of camptodactyly this model covers, and on what evidence? provenance

Typical measurements

Recalled without web access and unsourced; every item is a lead to verify.

  1. Which of these typical measurements hold for the sense of camptodactyly this model covers, and on what evidence? provenance

Failure modes and hazards

Recalled without web access and unsourced; every item is a lead to verify.

  1. Which of these failure modes and hazards hold for the sense of camptodactyly this model covers, and on what evidence? provenance

Neighbouring kinds and how to tell them apart

Recalled without web access and unsourced; every item is a lead to verify.

  1. Which of these neighbouring kinds and how to tell them apart hold for the sense of camptodactyly this model covers, and on what evidence? provenance

Classifiers Filled

Family
Thing Registry
Category
Cross-cutting context
Entry kind
thing
Plane
XCT
Domain
XCT.STA
Other names and narrower kinds
camptodactyly-ichthyosis syndrome, Spondylocamptodactyly syndrome

What it is Filled

Camptodactyly is a usually painless, nontraumatic flexion contracture of a finger's proximal interphalangeal joint, most often affecting the little finger, that may occur in isolation or as part of a syndrome.

In scope

  • Affected fingers, hands and joint-level flexion pattern
  • Active extension deficit and passive correctability
  • Age at recognition, growth-related changes and longitudinal progression
  • Hand function, symptoms and patient priorities
  • Evidence for isolated, familial or syndromic presentation
  • Clinician-directed management and measured outcomes

Out of scope

  • Complete models of syndromes that include camptodactyly
  • Clinodactyly and other primarily sideways finger deviations
  • Acquired contractures attributable to trauma, burns or inflammatory disease
  • Trigger digit and other distinct tendon disorders
  • Detailed surgical techniques and orthosis manufacturing specifications

Why it exists Filled

Enable an agent to recognise camptodactyly, record finger-specific severity and progression, and support clinician-led decisions about observation, therapy and specialist assessment.

Distinguishing features Filled

  • Establish whether the principal deformity is flexion at the proximal interphalangeal joint rather than sideways deviation characteristic of clinodactyly.
  • Measure active and passive extension separately: passive correction can remain possible, so rigidity is not a required recognition criterion.
  • Investigate injury, scarring, inflammation or another acquired explanation before classifying a bent finger as camptodactyly.
  • Record the affected joints and any catching or locking to distinguish persistent PIP flexion from a trigger digit presentation.
  • Treat little-finger involvement as supportive rather than mandatory; other fingers and both hands may be affected.

What robots and AI may and may not do Filled

Must not

  • Diagnose the condition from photos in place of a clinician.
  • Speculate that a named person has a syndrome because of a bent finger.
  • Share hand images or medical records without consent.

Only with a human decision

  • Any decision about splinting or surgery.

May

  • Explain the condition from medical references.
  • Help a person find hand specialists or support.

Moral aspects Filled

  • Visible differences can draw unwanted attention, especially for children.

Who is affected

  • People with the condition
  • Children and their parents

Owners Filled

Steward

Nobody owns the condition; each patient's records are kept by their healthcare provider.

Links to other meta-models Filled

parent

  • Q55787044 - registry parent class

What else AI and robots need to interact with it Filled

Identity and identifiers required Filled

  • Vercy registry: vr.tr.camptodactyly
  • Wikidata: Q614013 (https://www.wikidata.org/wiki/Q614013)

Direct properties not applicable Not applicable

  • Affected digit and joint distribution: Left/right hand; digit; PIP and any additional involved joints
  • Active PIP extension deficit: Degrees short of full extension, with examination position recorded
  • Passive PIP extension deficit: Degrees short of full extension under examiner-assisted movement
  • Available finger flexion: Joint-specific degrees and ability to complete a functional fist
  • Onset and recognition: Present at birth; infancy; adolescence; other; unknown, with age first observed
  • Contracture trajectory: Stable; worsening; improving; recurrent; insufficient comparable observations
  • Functional interference: Task-specific difficulty, assistance, avoidance and patient-reported burden
  • Associated condition: No association identified; suspected syndrome; confirmed syndrome, with evidence
  • Management exposure: Observation; prescribed stretching; splinting; hand therapy; surgery, with dates

Plane XCT: no invented physical properties.

Recognition optional Filled

  • A finger, most often the little finger, bent at its middle joint that cannot fully straighten.

Capabilities and actions required Filled

  • Create a finger-by-finger record of posture, movement and diagnostic confidence.
  • Compare serial extension and flexion measurements under documented examination conditions.
  • Identify unresolved differential diagnoses or associated findings requiring clinician review.
  • Track prescribed therapy, tolerability and barriers to completion.
  • Prepare a specialist review summary linking progression, task limitations and treatment response.
  • Evaluate outcomes against patient priorities while recording residual deformity or lost motion.

Hazards and failure modes required Filled

  • Severe cases can limit grip and hand function.

Standards and interfaces required Filled

  • The World Health Organization International Classification of Diseases, Tenth Revision, includes congenital camptodactyly under Q68.1, congenital deformity of hand.

Context of use required Filled

  • Camptodactyly is encountered in assessments of finger posture, hand function and congenital limb differences.
  • Clinical documentation distinguishes isolated involvement from cases associated with broader syndromes and records changes during growth.

Sources Filled

  1. Wikidata item Q614013: camptodactyly - identity and sense of the item
  2. Wikipedia: Camptodactyly - general description of the item

Open questions

  • Which diagnostic criteria most reliably separate camptodactyly from other causes of persistent PIP flexion across age groups?
  • Which examination positions and measurement methods provide reproducible active and passive extension measurements?
  • How well do age, passive correctability and digit distribution predict progression during growth?
  • Which associated findings justify genetic assessment, and what evidence supports that referral threshold?
  • Which treatment indications and patient-reported outcome measures have sufficient evidence to compare observation, therapy and surgery over long-term follow-up?

Machine files

Provenance

thing registry research (pass 2) · unreviewed

Built from: models/things/publications/thing-q614013/spec.json