Developmental delay with autism spectrum disorder and gait instability is a rare, genetic, neurological disorder characterized by infant hypotonia and feeding difficulties, global development delay, mild to moderated intellectual disability, delayed independent ambulation, broad-based gait with arms upheld and flexed at the elbow with brisk walking or running, and limited language skills. Behavior patterns are highly variable and range from sociable and affectionate to autistic behavior.
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microcephaly and chorioretinopathy
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microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
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autosomal dominant primary microcephaly
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Prader-Willi syndrome
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Smith-Magenis syndrome
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microcephalic osteodysplastic primordial dwarfism type I
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