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Zinsser-Cole-Engmann syndrome.

Q Masood¹, S Manzoor, I Hussain

¹Department of Dermatology, STD and Leprosy, Government Medical College and Associate SMHS Hospital, Srinagar, Kashmir, J & K, India.

Indian Journal of Dermatology, Venereology and Leprology

|August 1, 2007

Summary

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Zinser-Cole-Engmann syndrome is a rare genetic disorder. This report details a unique case, highlighting its characteristic skin, nail, and oral symptoms.

Area of Science:

Dermatology
Genetics
Oral Medicine

Background:

Zinser-Cole-Engmann syndrome is an exceptionally rare condition.
It is defined by a specific triad of clinical manifestations.

Purpose of the Study:

To report a clinical case of Zinser-Cole-Engmann syndrome.
To contribute to the limited literature on this rare entity.

Main Methods:

Case report presentation.
Clinical examination and documentation.

Main Results:

The patient presented with the hallmark features of Zinser-Cole-Engmann syndrome.
These included skin atrophy and pigmentation, nail dystrophy, and oral leukoplakia.

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Conclusions:

This case underscores the diagnostic criteria for Zinser-Cole-Engmann syndrome.
Further case reports are valuable for understanding this rare disorder.