Clouston Syndrome: 25-year follow-up of a patient
AUTOR(ES)
Trídico, Lívia Arroyo, Antonio, João Roberto, Pozetti, Eurides Maria de Oliveira, Rosa, Ana Maria Mendes, Antonio, Carlos Roberto
FONTE
An. Bras. Dermatol.
DATA DE PUBLICAÇÃO
2015-12
RESUMO
Abstract: Clouston syndrome is a rare genodermatosis that affects skin and annexes. It is a form of ectodermal dysplasia characterized by generalized hypotrichosis, palmoplantar hyperkeratosis and nail dystrophy. This paper reports a 25-year follow-up of a patient with Clouston syndrome, from childhood to adulthood, monitoring diagnosis and clinical course of the disease.
Documentos Relacionados
- Mitral Valve Replacement and Limited Myectomy for Hypertrophic Obstructive Cardiomyopathy: A 25-Year Follow-Up
- Left Stellate Ganglionectomy for the Long Q-T Interval Syndrome: Nine-Year Follow-up of a Patient
- Reiter's syndrome: long-term follow-up data.
- Orthodontic-surgical treatment of a patient with Marfan Syndrome and Obstructive Sleep Apnea Syndrome: a case report with a 9-year follow-up
- Chronic Bronchitis: A Five-year Follow-up