Motor and speech disorders in classic galactosemia

Nancy L Potter1, Yves Nievergelt, Lawrence D Shriberg

  • 1Department of Speech and Hearing Sciences, Washington State University Spokane, 412 E. Spokane Falls Blvd., Spokane, WA, 99202-2131, USA, nlpotter@wsu.edu.

JIMD Reports
|April 3, 2013
PubMed

Insights

Children with classic galactosemia often experience speech, strength, and coordination issues. These co-occurring disorders suggest a common cause, possibly related to cerebellar damage.

Area of Science:

  • Neurology
  • Pediatrics
  • Genetics

Background:

  • Classic galactosemia is a metabolic disorder.
  • Speech disorders are common in children with galactosemia.
  • The co-occurrence of other neurological deficits is not well understood.

Purpose of the Study:

  • To investigate the hypothesis that children with classic galactosemia and speech disorders are at risk for co-occurring strength and coordination disorders.
  • To explore the relationship between speech errors, strength, coordination, and neonatal milk exposure in children with galactosemia.

Main Methods:

  • A case-control study involving 32 children with galactosemia and 130 controls, aged 4-16 years.
  • Speech was assessed using the Percentage of Consonants Correct (PCC).
  • Hand and tongue strength were measured using the Iowa Oral Performance Instrument, and coordination was assessed with the Movement Assessment Battery for Children.

Main Results:

  • Children with galactosemia exhibited weaker hand and tongue strength and significant coordination deficits, particularly in balance and manual dexterity.
  • Children with more severe speech errors (childhood apraxia of speech, ataxic dysarthria) showed poorer balance and manual dexterity.
  • Neonatal milk exposure correlated with increased speech errors in males but not females.

Conclusions:

  • Children with galactosemia have a high prevalence of co-occurring speech, coordination, and strength disorders.
  • These deficits may indicate a common underlying etiology, potentially diffuse cerebellar damage.
  • Early identification and intervention for these co-occurring disorders are crucial for affected children.

Related Concept Videos

Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Gastrointestinal Motility Disorders01:20

Gastrointestinal Motility Disorders

Gastrointestinal or GI motility disorders are characterized by irregular gastrointestinal tract movements, disrupting food transit from the mouth to the anus. They are caused by damage or dysfunction in gut muscles or nerves. These disorders can cause symptoms such as severe constipation, diarrhea, abdominal pain, and swallowing difficulties. Disorders can affect any segment of the GI tract and range widely in severity, from common conditions like GERD to life-threatening conditions like...
Disorders of the Skeletal Muscle01:28

Disorders of the Skeletal Muscle

The clinical conditions affecting the skeletal muscle tissue are broadly categorized as musculoskeletal and neuromuscular disorders.
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
Myasthenia Gravis ll: Pathophysiology01:22

Myasthenia Gravis ll: Pathophysiology

The disease process of myasthenia gravis begins at the neuromuscular junction, where antibodies attack key proteins needed for muscle activation. This immune reaction weakens signal transmission, leading to the characteristic muscle fatigue and weakness that define the condition.Immune-Mediated DamageIn most individuals, antibodies target acetylcholine receptors (AChRs) on the postsynaptic membrane of muscle cells. By blocking acetylcholine binding, these antibodies prevent the nerve signal...
Alterations in Muscle Tone ll01:12

Alterations in Muscle Tone ll

Alterations in muscle tone are common manifestations of neurological disorders and reflect dysfunction within different nervous system regions. Spasticity, paratonia, and dystonia represent distinct forms of hypertonia, each with unique mechanisms, clinical features, and diagnostic importance.CharacteristicsSpasticity happens from upper motor neuron lesions and is characterized by velocity-dependent resistance to passive movement. Clinical features include:Exaggerated deep tendon reflexesClonus...