Nephrotic syndrome with often-early onset defined by severe proteinuria with low serum albumin and possible oedema. This disease is rare but severe as it usually progresses to end-stage renal failure. Mutations in the NPHS2 gene (chromosome 1q25-q31

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syndrome néphrotique idiopathique familial cortico-résistant

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A very rare secondary neonatal autoimmune disease characterised by generalised weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrop

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dermatomyosite néonatale

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A rare gastrooesophageal disease characterised by diffusely enlarged gastric folds, excessive mucus secretion, normal serum protein and gastric TGF-alpha levels. Patients typically present anaemia, abdominal pain not related to eating or bowel habits

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gastropathie hypertrophique sans hypoprotéinémie

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D'autres ont cherché : pirquet serum disease anti-foot-and-mouth disease serum serum against allergic diseases serum disease serum intoxication serum reaction serum sickness Pirquet serum disease

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Date index: 2023-10-19