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Results 1 - 8 of 8 for Weight loss center
  1. CA5A gene 
    ... potentially life-threatening episodes of poor feeding, vomiting, weight loss, tiredness (lethargy), rapid breathing (tachypnea), seizures, or coma. ...
    https://medlineplus.gov/genetics/gene/ca5a - Genetics
  2. Carbonic anhydrase VA deficiency 
    ... life-threatening episodes can cause poor feeding, vomiting, weight loss, tiredness (lethargy), rapid breathing (tachypnea), seizures, or coma. ...
    https://medlineplus.gov/.../carbonic-anhydrase-va-deficiency - Genetics
  3. SLC35A2-congenital disorder of glycosylation 
    ... feeding difficulties and fail to grow or gain weight at the expected rate. Some have vision or hearing problems.In SLC35A2-CDG, medical imaging shows loss of tissue (atrophy) in parts of the brain ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  4. Combined oxidative phosphorylation deficiency 1 
    ... time; they also have difficulty growing and gaining weight at the expected rate (failure to thrive). In some cases, affected individuals have abnormal muscle tone (increased or decreased), developmental delay, seizures, loss of sensation in the limbs (peripheral neuropathy), and ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  5. Combined malonic and methylmalonic aciduria 
    ... developmental delay, an inability to grow and gain weight at the expected rate ... such as seizures, loss of memory, a decline in thinking ability, or ...
    https://medlineplus.gov/...mbined-malonic-and-methylmalonic-aciduria - Genetics
  6. CAV1 gene 
    ... and symptoms of this condition include an overall loss of body fat except in the buttocks and on the palms of the hands and soles of the feet. Additional features include thin skin with visible blood vessels; a large, triangular head; and slow weight gain in childhood. The CAV1 gene mutations that ...
    https://medlineplus.gov/genetics/gene/cav1 - Genetics
  7. Russell-Silver syndrome 
    ... Le Bouc Y. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  8. RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy 
    ... DNA or mtDNA). Mitochondria are the energy-producing centers in cells, and the DNA in these structures ...
    https://medlineplus.gov/...halomyopathic-form-with-renal-tubulopathy - Genetics