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Language in genetic syndromes, intellectual disability and selective mutism

In intellectual disability language develops in the usual order but slowly, and each syndrome creates its own profile — in Down syndrome syntactic expression is weaker than comprehension, in Williams syndrome vocabulary and social drive are relatively strong — while selective mutism is an anxiety disorder in which the child speaks at home and is silent elsewhere.

Why it matters in the exam

Exam questions ask you to match a profile to a syndrome: what will be hard for a child with Down syndrome (producing a long noun phrase with an embedded clause); what characterises a child with Williams syndrome (good vocabulary and social drive, with visuospatial difficulty); and which of the syndromes once grouped under "pervasive developmental disorders" has a known genetic basis (Rett). You are also asked that in mild to moderate intellectual disability language develops in the usual order, more slowly, and that different syndromes affect language in different ways.

Selective mutism is presented as a preschool girl whose home videos show normal, fluent talk, while at kindergarten she has stayed silent for many months, even with staff she knows. The diagnosis is selective mutism, and treatment is team-based with gradual exposure. For differential diagnosis you may also be asked about an 18-month-old who does not respond to speech: think of severe hearing loss and of autism.

Key points

Summary table

ConditionLanguage and communication profileExam point
Mild to moderate intellectual disabilityThe usual order of acquisition, but slowThe profile depends on the syndrome
Down syndromeExpression and syntax weaker than comprehension and vocabulary; low intelligibility; hypotoniaHigh rate of middle ear fluid — check hearing
Williams syndromeGood vocabulary and strong social drive, visuospatial difficultyA profile "opposite" to Down syndrome in some areas
Fragile X syndromePerseveration, fast disorganised speech, gaze avoidance, social anxietyMore common in boys
Rett syndromeRegression in communication and hand use, repetitive hand movementsA known genetic basis (MECP2), mainly in girls
Selective mutismSpeaks freely in one place and is silent in others over time, normal languageAn anxiety disorder; team and gradual exposure

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Sources

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Reviewed by the Examqo AI Professor · 2026-11-02. The text may contain errors; when in doubt, check the source.