التفاصيل البيبلوغرافية
| العنوان: |
Ichthyosis prematurity syndrome mimics keratitis–ichthyosis–deafness syndrome at birth: Use of electron microscopy and genetic testing. |
| المؤلفون: |
Youssef, Molly J., Wolz, Michael M., Harris, Malinda N., Richard, Gabrielle, Bridges, Alina G., Wieland, Carilyn N., Hand, Jennifer L. |
| المصدر: |
International Journal of Dermatology; Aug2016, Vol. 55 Issue 8, pe454-e457, 4p, 3 Color Photographs |
| مصطلحات موضوعية: |
ICHTHYOSIS, KERATOSIS, INFANT health services, ELECTRON microscopy, PATIENT acceptance of health care, HEALTH outcome assessment, PATIENTS, DIAGNOSIS |
| مستخلص: |
The article presents a case study of an infant boy who was born to nonconsanguineous parents of Norwegian and German/ Irish descent. The infant was diagnosed with keratitis-ichthyosis-deafness (KID) syndrome. The infant had respiratory distress at birth. The infant receives humidified air and petrolatum ointment as treatment for the skin disease. |
| قاعدة البيانات: |
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