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[Prassad syndrome--case report]

E Sayali1, M Canbakan, E Arikan

  • 12. Klinik der Inneren Medizin-Taksim, Istanbul, Türkei.

Wiener Medizinische Wochenschrift (1946)
|January 1, 1996
PubMed
Summary

Prassad syndrome, a rare condition, is characterized by growth retardation, hypogonadism, and organomegaly. This case report details the diagnosis of Prassad syndrome in a patient presenting with these distinct features.

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Area of Science:

  • Pediatric Endocrinology
  • Clinical Genetics
  • Gastroenterology

Background:

  • Prassad syndrome is a rare genetic disorder with a complex presentation.
  • Key features include growth retardation, hypogonadism, and hepatosplenomegaly.

Observation:

  • The case report details a patient diagnosed with Prassad syndrome.
  • The patient exhibited characteristic symptoms such as zinc and iron deficiency, geophagia, and altered small intestinal mucosa.

Findings:

  • Diagnosis of Prassad syndrome was confirmed in the presented case.
  • The patient's clinical presentation aligned with the known features of this rare syndrome.

Implications:

  • Highlights the importance of recognizing the multifaceted symptoms of Prassad syndrome.

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  • Contributes to the limited case data available for this rare disorder.
  • Emphasizes the need for comprehensive diagnostic approaches in patients with unexplained growth and developmental issues.