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The 20 pages that link to Developmental delay, each with the reason it gives.
Chromosomal microarrayRelated: Microarray is commonly used to investigate unexplained developmental delay for genomic gains and losses.
Developmental screeningRelated: Developmental delay is one of the concerns screening is designed to detect.
HypotoniaRelated: Persistent hypotonia can coexist with delayed motor development and prompt broader assessment.
MicrocephalyRelated: Monitoring development helps identify support needs that head measurements cannot establish.
Bardet–Biedl syndromeRelated: Developmental differences can accompany the physical and sensory features of BBS.
HomocystinuriaRelated: Neurological effects may include delayed development, especially in untreated disease.
Sotos syndromeRelated: Delays in motor, language, or cognitive development commonly accompany Sotos syndrome.
MacrocephalyRelated: Its presence alongside macrocephaly can suggest an underlying neurological or genetic condition.
Sturge–Weber syndromeRelated: Extensive or early brain involvement may affect developmental progress.
1p36 deletion syndromeRelated: It is a frequent early concern in affected children.
Pentasomy XRelated: Developmental delay is commonly reported and can guide early intervention.
Smith–Magenis syndromeRelated: Delays in speech, motor skills, and learning often prompt developmental assessment.
Tetrasomy XRelated: Developmental differences are among the reasons children with tetrasomy X may be assessed.
Developmental disorderRelated: Delay can be an early sign of a disorder, though it does not by itself establish a diagnosis.
Infantile epileptic spasms syndromeRelated: Developmental delay is common, but its extent differs widely among affected children.
Oculocerebrorenal syndromeRelated: Developmental assessment guides educational and supportive care for neurological impairment.
Pitt–Hopkins syndromeRelated: It is a defining feature, often affecting speech, movement, and learning.