Rare Diseases Symptoms Automatic Extraction

Neonatal erythroderma: diagnostic and therapeutic challenges.

[omenn syndrome]

Erythroderma a life-threatening entity during the first one month, and many a time, a manifestation of genodermatosis, immune deficiency, psoriasis, metabolic diseases, and infections. Atopic dermatitis presenting as erythroderma is usually observed later, after this one-month period, and hence not a common differential for neonatal exfoliative dermatitis. Although a rare entity, there is a paucity of studies on this and in contrast to adults, some may manifest as cardinal signs of primary disease conditions.

Diseases presenting "immune deficiency" symptom

  • 22q11.2 deletion syndrome
  • congenital diaphragmatic hernia
  • oculocutaneous albinism
  • omenn syndrome
  • pyomyositis
  • severe combined immunodeficiency
  • typhoid
  • wiskott-aldrich syndrome

This symptom has already been validated