Journals / Medical Journal of Ege University / 1999 / Cilt: 9 - Sayı: 2

Hypohidrotic ectodermal dysplasia: Case reports

Pages
45–48
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Most affected children require extensive dental treatment to restore their appearance and promote normal growth and development.

📌 3 Key Takeaways

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Objective & Hypothesis:Hypohidrotic ectodermal dysplasia is a rare congenital syndrome which affects ectodermal structures.
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Key Findings & Data:It is usually transmitted as an X-linked recessive trait.
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Conclusion & Impact:Most affected children require extensive dental treatment to restore their appearance and promote normal growth and development.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Ektodermal displazi · Deri anomalileri · Deri hastalıkları

Abstract

Hypohidrotic ectodermal dysplasia is a rare congenital syndrome which affects ectodermal structures. It is usually transmitted as an X-linked recessive trait. Rarely it can be transmitted autosomal recessively. Manifestations of this disorder may include teeth, skin, hair, nails and sweat glands. Most affected children require extensive dental treatment to restore their appearance and promote normal growth and development.

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Cite This Article

ÖNÇAĞ, Ö., ELBEK, Ç., ÖZKINAY, F. (1999). Hypohidrotic ectodermal dysplasia: Case reports. Medical Journal of Ege University, Cilt: 9 - Sayı: 2, 45–48. https://ajindex.com/articles/283080