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Research draft

ptosis

vr.tr.ptosis · INF.KNW

Let an agent explain eyelid ptosis and its causes in general terms from ophthalmic sources, identify urgent presentations, describe treatment, distinguish ptosis from other eyelid and brow conditions, and route personal questions to clinicians.

Thing Registry Information and virtual systems

Research draft, second pass

A second pass drafted this model: the structure a model of this thing needs, and what is known about it in the world. The line under this one says how the second half was obtained - researched against sources, or recalled without web access, in which case nothing here was read anywhere and every claim is a lead to verify. Unreviewed either way.

written by Claude from model knowledge without web access - no source was read, every claim is a lead to verify

Researched by: Claude

Purpose and description

Let an agent explain eyelid ptosis and its causes in general terms from ophthalmic sources, identify urgent presentations, describe treatment, distinguish ptosis from other eyelid and brow conditions, and route personal questions to clinicians.

Drooping of the upper eyelid, present from birth as congenital ptosis or acquired through ageing, muscle or nerve disorders such as myasthenia gravis, third nerve palsy, Horner syndrome and myotonic dystrophy, trauma or long-term contact lens use, and occurring as a feature of syndromes such as Borjeson-Forssman-Lehmann, Jacobsen syndrome, mucopolysaccharidosis II and dopamine beta-hydroxylase deficiency, or with unusual movement as in jaw-winking syndrome; ptosis can block vision in children and is treated by surgery when needed.

What it is for: Not applicable; a clinical sign.

It can be explain causes; identify urgent presentations; relay treatment; route personal questions.

Distinguishing features

Eyelid drooping

Many causes

Congenital and acquired

Vision impact in children

What it looks like

A drooping upper eyelid covering part of the eye.

Physical character

congenital ptosis incidence: about 1 in 800 births - estimates

normal upper lid position: about 1-2 mm below the limbus measure

How it is recognised

Drooping upper eyelid

Congenital, aponeurotic, myogenic, neurogenic and mechanical ptosis; syndromic ptosis; jaw-winking

Dermatochalasis is excess skin; brow ptosis is a drooping brow; the word ptosis also names drooping of other organs

Related models

is a kind of - in registry terms

eyelid disease

is a kind of - in registry terms

general symptom

is a kind of - in registry terms

eye disease

is caused by - among other conditions

myasthenia gravis

In practice

Families and kinds

congenital ptosis

aponeurotic or involutional ptosis of ageing

myogenic ptosis in myasthenia gravis and myotonic dystrophy

neurogenic ptosis in third nerve palsy and Horner syndrome

mechanical and traumatic ptosis

syndromic ptosis in conditions such as Borjeson-Forssman-Lehmann, Jacobsen, mucopolysaccharidosis II and dopamine beta-hydroxylase deficiency

Marcus Gunn jaw-winking syndrome

Identifiers

ICD-11 9A01.3 ptosis of eyelid

MeSH D001763 blepharoptosis

Standards and regulation

Ophthalmology guidelines on ptosis assessment and surgery

Paediatric vision screening guidance

Failure modes and hazards

Missing sudden ptosis from aneurysm or stroke

Amblyopia in children with untreated ptosis

Agents giving personal medical advice

Registry aliases naming whole syndromes as ptosis

Also called

Borjeson-Forssman-Lehmann syndromedopamine beta-hydroxylase deficiencyjaw-winking syndromemucopolysaccharidosis IIJacobsen syndromemyotonic dystrophycongenital ptosisChar syndromeOculopharyngodistal myopathyptosis-strabismus-ectopic pupils syndromeptosis-vocal cord paralysis syndromeblepharophimosis-ptosis-esotropia-syndactyly-short stature syndromeAcrootoocular syndromeoculogastrointestinal muscular dystrophyatrioventricular defect-blepharophimosis-radial and anal defect syndromeblepharophimosis-radioulnar synostosis syndromeptosis-upper ocular movement limitation-absence of lacrimal punctum syndromeMarin-Amat syndromeInverse Marcus-Gunn phenomenonmucopolysaccharidosis type 2, severe formmucopolysaccharidosis type 2, attenuated formoculopharyngodistal myopathy 4

Where this came from

wikidata · CC0 1.0

Drafted structure

Bundle to layer to finding to question, as the second pass will find it: 4 bundles · 8 layers · 8 findings · 16 questions.

Help Urgent signs first.

Safety.

Urgent

Sudden ptosis.

Urgent

Urgent.

  1. Why does sudden ptosis with double vision, an enlarged pupil, headache or weakness need emergency care? action
  2. Is the user describing sudden ptosis with such signs, which need emergency services now? boundary

Assessment

Assessment.

Assessment

Assessment.

  1. How do clinicians assess ptosis and find its cause, in general terms? provenance
  2. Is the user asking about their own eyelid, which needs a clinician? boundary
Understand The sign.

Clinical.

Definition

Definition.

Definition

Definition.

  1. What is ptosis, and how does it differ from dermatochalasis and brow ptosis? definition
  2. Is the question about eyelid ptosis or drooping of another organ? boundary

Causes

Causes.

Causes

Causes.

  1. What causes ptosis, from ageing and nerve palsies to myasthenia and syndromes such as Borjeson-Forssman-Lehmann and Jacobsen? provenance
  2. Which entry fits the specific cause? action
Treat Treatment.

Clinical.

Treatment

Treatment.

Treatment

Treatment.

  1. How is ptosis treated by surgery or by treating the cause, per guidelines? provenance
  2. Which references are standard? provenance

Children

Children.

Children

Children.

  1. Why does congenital ptosis need monitoring for amblyopia, and when is surgery done? provenance
  2. Which sources are cited? provenance
Context Special forms and history.

Context.

Special

Jaw-winking and syndromes.

Special

Special.

  1. What are Marcus Gunn jaw-winking syndrome and the syndromes that include ptosis? provenance
  2. Which entry fits the specific syndrome? action

History

History.

History

History.

  1. How has ptosis surgery developed? provenance
  2. Which entry fits the history of ophthalmology? action

What the second pass must settle

  • Should congenital ptosis and myasthenia gravis be separate primary entries?
  • How should clinical guidelines be linked?
  • The registry entry has merged aliases naming syndromes in which ptosis is one feature; should they be split off?