Adenosine deaminase deficiency

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Adenosine deaminase deficiency

NBME

NBME

Amino acid metabolism
Nitrogen and urea cycle
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Gluconeogenesis
Glycogen metabolism
Glycolysis
Pentose phosphate pathway
Physiological changes during exercise
Cholesterol metabolism
Fatty acid oxidation
Fatty acid synthesis
Ketone body metabolism
Alkaptonuria
Cystinuria (NORD)
Hartnup disease
Homocystinuria
Maple syrup urine disease
Ornithine transcarbamylase deficiency
Phenylketonuria (NORD)
Essential fructosuria
Galactosemia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hereditary fructose intolerance
Lactose intolerance
Pyruvate dehydrogenase deficiency
Abetalipoproteinemia
Familial hypercholesterolemia
Hyperlipidemia
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Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Fabry disease (NORD)
Gaucher disease (NORD)
Krabbe disease
Leukodystrophy
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Niemann-Pick disease type C
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Tay-Sachs disease (NORD)
Cystinosis
Disorders of amino acid metabolism: Pathology review
Disorders of carbohydrate metabolism: Pathology review
Disorders of fatty acid metabolism: Pathology review
Dyslipidemias: Pathology review
Glycogen storage disorders: Pathology review
Lysosomal storage disorders: Pathology review
Carbohydrates and sugars
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Iodine deficiency
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Wernicke-Korsakoff syndrome
Fat-soluble vitamin deficiency and toxicity: Pathology review
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Zinc deficiency and protein-energy malnutrition: Pathology review
Cell membrane
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Nernst equation
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DNA cloning
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Amino acids and protein folding
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Gene regulation
Lac operon
Mitosis and meiosis
Nuclear structure
Nucleotide metabolism
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Transcription of DNA
Translation of mRNA
Adenosine deaminase deficiency
Lesch-Nyhan syndrome
Orotic aciduria
Bloom syndrome
Fanconi anemia
Li-Fraumeni syndrome
McCune-Albright syndrome
Xeroderma pigmentosum
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Purine and pyrimidine synthesis and metabolism disorders: Pathology review
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Antimetabolites: Sulfonamides and trimethoprim
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Cell wall synthesis inhibitors: Cephalosporins
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Introduction to pharmacology
Enzyme function
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Pharmacodynamics: Agonist, partial agonist and antagonist
Pharmacodynamics: Desensitization and tolerance
Pharmacodynamics: Drug-receptor interactions
Pharmacokinetics: Drug absorption and distribution
Pharmacokinetics: Drug elimination and clearance
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ACE inhibitors, ARBs and direct renin inhibitors
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Hypoglycemics: Insulin secretagogues
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High Yield Notes

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Adenosine deaminase deficiency

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Questions

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A 6-month-old girl is brought to the physician due to persistent diarrhea for months. She has been hospitalized three times in the last two months due to respiratory infections that required intravenous antibiotics. Temperature is 37.8°C (100°F), blood pressure is 98/56 mmHg, and pulse is 110/min. On physical examination, the tonsils are absent. An eczematous rash is noticed over the face, limbs, and trunk. She is at the 4th percentile for weight and 5th percentile for height. Both parents are healthy; however, the patient had a brother who died at the age of two due to a severe respiratory infection. Laboratory testing is shown below. Which of the following best explains this patient's condition?

Laboratory Value  Result 
 Hemoglobin   10 g/dL 
 Mean corpuscular volume  90 fL 
 Neutrophil count  1000/mm3  
 T lymphocyte count   300/mm3 
 B lymphocyte count   170/mm3 
 Platelet count   160,000/mm3 

External References

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Adenosine deaminase deficiency p. 35, 115

Autosomal recessive disorders

adenosine deaminase deficiency p. 115

SCID (severe combined immunodeficiency disease) p. 96, 115

adenosine deaminase deficiency as cause p. 35

Transcript

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Adenosine deaminase deficiency, or ADA deficiency, is a rare genetic disease, that results in severe combined immunodeficiency, or SCID for short.

SCID can be caused by a number of causes, so this particular variation is called ADA-SCID.

Let’s take a step back. Our cells have all the instructions on how to live and behave written on their own copy of DNA.

DNA is made out of four nucleotides, which can also do all kinds of cool stuff in their free time, like provide energy to various processes in the cell.

Nucleotides are made out of a sugar, in this case deoxyribose, one to three phosphate groups, and a nucleobase, which can be adenine, thymine, cytosine, or guanine.

So, the name of a deoxyribose-containing, triphosphatic nucleotide, based on adenine, that makes up DNA would be deoxyadenosine triphosphate, or dATP, for short.

These nucleotides are needed in equal proportions in order to make cellular division run smoothly.

Now, nucleotides have a functional lifetime of their own, and our body has mechanisms on how to break them up into their building blocks, to be either excreted or recycled.

Let’s focus on deoxyadenosine triphosphate.

First the enzyme adenosine deaminase removes an amine group from it, turning it into deoxyinosine monophosphate, or dIMP.

Then purine nucleoside phosphorylase comes in and removes the phosphate and the deoxyribose from dIMP, making hypoxanthine.

Hypoxanthine is then oxidised twice by xanthine oxidase - first to become xanthine, and then finally, to uric acid.

Uric acid can then be excreted by the kidneys, in the form of urine.

Now one class of cells that divides quickly and therefore relies heavily on cell division to work smoothly are lymphocytes.

Lymphocytes protect the body from pathogens, like bacteria and viruses in two ways.

First, B lymphocytes, or B cells, produce immune proteins called antibodies, which seek out and latch on onto an invader, marking it for destruction by other cells.

Second, cytotoxic T lymphocytes, or cytotoxic T cells, as well as lymphocytes called natural killer cells, go cell to cell, looking for virally-infected cells or cells that look like they’ve started dividing uncontrollably - like a cancer cell.

If they find a cell like that, they destroy it.

Simultaneous breakdown of both of these pathways makes the immunodeficiency combined, and severe.

Hence the name, severe combined immunodeficiency.

Adenosine deaminase is encoded by a gene on chromosome 20, and typically mutations are inherited through an autosomal recessive pattern, meaning that the disease occurs when a child receives a mutant allele from both parents.

Sources

  1. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  2. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  3. "Yen & Jaffe's Reproductive Endocrinology" Saunders W.B. (2018)
  4. "Bates' Guide to Physical Examination and History Taking" LWW (2016)
  5. "Robbins Basic Pathology" Elsevier (2017)
  6. "Adenosine deaminase deficiency: Frequency and comparative pathology in autosomally recessive severe combined immunodeficiency" Clinical Immunology and Immunopathology (1979)
  7. "Educational paper" European Journal of Pediatrics (2011)
  8. "Development of gene therapy: potential in severe combined immunodeficiency due to adenosine deaminase deficiency" Stem Cells and Cloning: Advances and Applications (2009)
  9. "Management options for adenosine deaminase deficiency; proceedings of the EBMT satellite workshop (Hamburg, March 2006)" Clinical Immunology (2007)