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Results 1 - 9 of 9 for Abnormally slow thought process
  1. CACNA1D gene 
    ... and deafness (SANDD), which is characterized by an abnormally slow and irregular heartbeat (bradycardia and arrhythmia) and hearing ...
    https://medlineplus.gov/genetics/gene/cacna1d - Genetics
  2. Gnathodiaphyseal dysplasia 
    ... long bones in the arms and legs is abnormally hard and thick (diaphyseal ... loose teeth, and slow healing after teeth are lost or extracted. Areas ...
    https://medlineplus.gov/.../condition/gnathodiaphyseal-dysplasia - Genetics
  3. Erdheim-Chester disease 
    ... to production of a BRAF protein that is abnormally active, which disrupts regulation of cell growth and ...
    https://medlineplus.gov/genetics/condition/erdheim-chester-disease - Genetics
  4. Noonan syndrome with multiple lentigines 
    ... to the production of a protein that functions abnormally, which impairs the protein's ability to respond ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  5. CDKN1C gene 
    ... Some of these genetic changes lead to an abnormally short, nonfunctional version of the CDKN1C protein, while ... of the body. The condition is characterized by slow growth before and after birth, skeletal abnormalities, hormonal ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  6. CHARGE syndrome 
    ... size and location. Some affected individuals also have abnormally small or underdeveloped eyes (microphthalmia). In many people ... the disorder. The minor characteristics include heart defects; slow growth starting in late infancy; delayed development of ...
    https://medlineplus.gov/genetics/condition/charge-syndrome - Genetics
  7. Mitochondrial DNA 
    ... and MT-TE gene mutations associated with MIDD slow protein production in mitochondria and impair their function. ... the cytochrome b protein or lead to an abnormally short protein. These cytochrome b alterations impair the ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  8. TBXAS1 gene 
    ... in the narrowing of blood vessels (vasoconstriction) to slow blood flow and the clumping (aggregation) of blood ... Ghosal hematodiaphyseal dysplasia. This condition is characterized by abnormally thick bones and a shortage of red blood ...
    https://medlineplus.gov/genetics/gene/tbxas1 - Genetics
  9. Primary familial brain calcification 
    ... of movement abnormalities called parkinsonism, which include unusually slow movement (bradykinesia), muscle rigidity, and tremors. Other movement ... calcification. The altered signaling may result in an abnormally large amount of calcium entering the cells that ...
    https://medlineplus.gov/.../primary-familial-brain-calcification - Genetics