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  2. Hypotonia - Wikipedia

    en.wikipedia.org/wiki/Hypotonia

    Severe hypotonia in infancy is commonly known as floppy baby syndrome. Recognizing hypotonia, even in early infancy, is usually relatively straightforward, but diagnosing the underlying cause can be difficult and often unsuccessful. The long-term effects of hypotonia on a child's development and later life depend primarily on the severity of ...

  3. RNU4-2 syndrome - Wikipedia

    en.wikipedia.org/wiki/RNU4-2_syndrome

    Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language (NEDHAFA) was a suggested name for this syndrome, however, ReNU syndrome (pronounced 'renew') was chosen through a collaboration between researchers and the families of those impacted by variants in RNU4-2. The name symbolises that this ...

  4. Congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Congenital_muscular_dystrophy

    The weakness is indicated as hypotonia, or lack of muscle tone, which can make an infant seem unstable. [1] [5] Eventually, most patients develop joint contractures or fixed joint deformities. [6] Children may be slow with their motor skills; such as rolling over, sitting up or walking, or may not even reach these milestones of life. Some of ...

  5. Multiple congenital anomalies-hypotonia-seizures syndrome

    en.wikipedia.org/wiki/Multiple_congenital...

    Multiple congenital anomalies-hypotonia-seizures syndrome is a rare multi-systemic genetic disorder which is characterized by developmental delay, seizures, hypotonia and heart, urinary, and gastrointestinal abnormalities.

  6. It's not just babies who need formula: Families of teens with ...

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  7. 1p36 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/1p36_deletion_syndrome

    1p36 deletion syndrome is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.

  8. Mitochondrial DNA depletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_DNA...

    In MDDS associated with mutations in TK2, infants generally develop normally, but by around two years of age, symptoms of general muscle weakness (called "hypotonia"), tiredness, lack of stamina, and difficulty feeding begin to appear. Some toddlers start to lose control of the muscles in their face, mouth, and throat, and may have difficulty ...

  9. Mental disorders diagnosed in childhood - Wikipedia

    en.wikipedia.org/wiki/Mental_disorders_diagnosed...

    In infants, some babies may be hypotonia, a loose and floppy baby, or hypertonia, a stiff and rigid baby. Toddlers may have trouble feeding themselves or may stand, sit or walk later than what is developmentally normal. Other signs of motor skills disorders may be children that are clumsy or have excessive accidents, such as knocking things over.