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Clinical case no. 1
A 55-year-old patient presents at the ED complaining of marked asthenia, vomiting, dark
urine (reddish-brown) and icterus (yellow) skin. From the patient's history it si noted: flu that
started 2weeks ago treated with paracetamol for 2weeks, dose of 5gr/24 hours (maximum
dose being 3gr/24 hours). Laboratory analyzes show increased values for GPT (5500 U/L),
GOT (5240 U/L), GGT (1025 U/L). Total Bilirubin (12 mg/dL) and Direct Bilirubin (5.8 mg/dL).
ALP is within normal limits.
Lp. 5
Clinical case no. 1
A 2-year-old child presents himself with his parents for a routine check-up at the family doctor.
He notes a sunken sternum, anterior fontanel not completely closed, and dental
demineralization. The parents stated that they administered vitamin D to the child daily. The
family doctor requests tests for total Calcium, Vitamin D3 and ALP. When dosing them, low
values below NV are observed.
Clinical case no. 2
A 25-year-old patient is brought by ambulance in the ED for: confusion, hallucinations,
convulsions, muscle weakness, signs of tetany, rhythm disorders. Laboratory analyzes show
normal values for Ca and low values for Mg.
Clinical case 1
The mother presents with a 1-year-old male child with white, sparse, fragile, wiry, curly hair,
who complains of convulsive seizures and si intellectually and physicaly delayed, and si smaller
for his age. Not working. Soft bones. Buccal facies, but muscle hypotonia and delayed
ostetendinous reflexes can be detected on touch. Karyotyping is carried out, as aresult of
which the change on the xchromosome si found. nI the antecedents, Fe treatment was
administered with good doses without response.
Laboratory tests:
• Fe (low)
• MCV - (low)
• MCH - low
• Cu - low
• ceruloplasmin - low
Clinical case 2
Woman with a 3-4 year old girl, minimal or asymptomatic signs, only hypochromic microcytic
anemia refractory to Fe treatment.
Laboratory tests:
• With - Low (easy)
• Fe - low
• ceruloplasmin - low
Clinical case 3
An adult patient presents to the doctor complaining of seizures, mild dysphagia, nausea,
marked asthenia, mild pain in the right hypochondrium. Greenish-yellow ring on the
periphery of the cornea, slight coordination disorder.
Heredocollateral antecedents: brother diagnosed with Wilson disease. Laboratory tests:
• does not show anemia
• GPT - Inc
• GOT - Inc
• ALP and GGT - can be Inc or Normal
• Urinary Cu - Inc (especially after administration of Cu chelators)
Clinical case no. 1
A 53-year-old patient presents to the doctor for: diffuse pain (muscular, bone), extreme fatigue,
loss ofappetite, weight gain, constipation, hair loss, rough hair, dry skin, brittle nails. The patient
is diagnosed with depression in the antecedents, but follows her treatment. Laboratory analyzes
indicate: T3, T4 (dec), TSH (Inc), Iodine (dec), Fe (dec) (hypochromic microcytic anemia), VitD
deficiency, LDL (Inc)
ESR = 10 mm/Hg
CP=340mg/dL (inc)
Presepsin = 100 ng/ml (Inc)
PCT=3.5ng/dL (inc)
Ferritin =200 ng/mL N
Fibrinogen = 580 mg/dL (Inc)
LDH=2250U/L (Inc)
TGP = 230 U/L (Inc)
TGO = 340 U/L (Inc)
Creatinine = 3.4 mg/dL (Inc)
Urea = 247 mg/dL (Inc)
Clinical case no. 2
A 65-year-old patient presents ot the hospital with pain in the ribs, spine, upper
and lower limbs.
Temperature =37°C, heart rate =83 BPM, respiratory rate =18 breaths/minute.