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Research draft

spina bifida

vr.tr.spina-bifida · XCT.STA

Let an agent explain spina bifida and its forms, relay causes, prevention, prenatal detection, treatment and living with the condition from medical and patient organisation sources in general terms, describe the forms the registry aliases name, and distinguish spina bifida from other neural tube defects and spinal conditions, respectfully and without personal medical advice.

Thing Registry Cross-cutting context

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 spina bifida and its forms, relay causes, prevention, prenatal detection, treatment and living with the condition from medical and patient organisation sources in general terms, describe the forms the registry aliases name, and distinguish spina bifida from other neural tube defects and spinal conditions, respectfully and without personal medical advice.

A neural tube defect in which the spinal column does not close completely during early fetal development, ranging from spina bifida occulta, a hidden and usually harmless gap, and congenital dermal sinus, to spina bifida cystica or aperta, including meningocele, where the membranes protrude, and myelomeningocele, where the spinal cord is involved, which can cause paralysis, hydrocephalus, bladder and bowel problems and hip problems; folic acid before and in early pregnancy reduces risk. The model gives general information and routes people to clinicians.

What it is for: Not applicable; a congenital condition.

It can be explain the forms; relay prevention and care; route to clinicians and support; distinguish related conditions.

Distinguishing features

Neural tube defect

Occult and open forms

Preventable in part

Lifelong care in severe forms

What it looks like

Not a visible object; in open forms a sac on the back at birth.

Physical character

prevalence: about 1 in 1000-2000 note - births, varies by country

folic acid risk reduction: up to about 70 percent

neural tube closure: about day 28 note - of gestation

How it is recognised

Incomplete closure of the spinal column

Spina bifida occulta, cystica, aperta, meningocele, congenital dermal sinus, hip problems

Anencephaly is another neural tube defect; scoliosis is spinal curvature; tethered cord can accompany spina bifida

Related models

is a kind of - in registry terms

neural tube defect

is a kind of - in registry terms

spinal dysraphism

is prevented in part by - supplementation

folic acid

is often associated with - in myelomeningocele

hydrocephalus

In practice

Families and kinds

spina bifida occulta

congenital dermal sinus

meningocele

myelomeningocele

associated hydrocephalus and Chiari II malformation

orthopaedic issues such as hip problems

Identifiers

ICD-10 Q05 spina bifida

MeSH D016135 Spinal Dysraphism

Standards and regulation

Folic acid fortification policies

Prenatal screening guidelines

Disability rights and education laws

Failure modes and hazards

Agents giving personal medical advice

Disrespectful framing of disability

Registry aliases mixing forms and complications

Also called

meningoceleCongenital dermal sinuship problems in spina bifidaspina bifida occultaspina bifida cysticaspina bifida apertacranial meningocelemyelocystocele

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.

Understand What spina bifida is.

Clinical.

Definition

Definition.

Definition

Definition.

  1. What is spina bifida, and how does it differ from other neural tube defects and spinal conditions? definition
  2. Is the question general, or about a pregnancy, a child or an adult s care, which needs clinicians? boundary

Forms

Forms.

Forms

Forms.

  1. What are spina bifida occulta, congenital dermal sinus, meningocele and myelomeningocele, and related hip problems? definition
  2. Which entry fits the specific form? action
Prevention Prevention and detection.

Regulation.

Folate

Folic acid.

Folate

Folate.

  1. What do health authorities recommend about folic acid and fortification? provenance
  2. Which references are standard? provenance

Prenatal

Prenatal detection.

Prenatal

Prenatal.

  1. How is spina bifida detected before birth, and what options are described in guidelines? provenance
  2. Which sources are cited? provenance
Care Treatment and living.

Clinical.

Treatment

Treatment.

Treatment

Treatment.

  1. What surgical and ongoing treatments exist, including fetal surgery, in general terms? provenance
  2. Which entry fits fetal surgery? action

Living

Living with spina bifida.

Living

Living.

  1. What do patient organisations say about daily life, education and independence? provenance
  2. Which entry fits spina bifida associations? action
Context Research and rights.

Context.

Research

Research.

Research

Research.

  1. What causes are being researched beyond folate? provenance
  2. Which entry fits neural tube defect research? action

Rights

Rights.

Rights

Rights.

  1. How do disability rights frameworks apply? provenance
  2. Is the presentation respectful? boundary

What the second pass must settle

  • Should meningocele and spina bifida occulta be separate primary entries?
  • How should medical and patient sources be linked?
  • The registry entry has merged aliases naming forms and complications; should they be split off?