Congenital Milroy Oedema: a case report of a family
| Autor: | Guarino R, L. Boscardini, P. Angellotti, G. Ballardini, Andrea Guala, Campra D, V. Raffa |
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| Rok vydání: | 2012 |
| Předmět: |
Male
Pathology medicine.medical_specialty lcsh:Surgery Edema congenito Disease Inheritance (object-oriented programming) hemic and lymphatic diseases Humans Medicine gene VEGFR3 Lymphedema sindrome di Milroy business.industry Milroy's disease lcsh:RJ1-570 Infant lcsh:Pediatrics lcsh:RD1-811 medicine.disease Dermatology humanities body regions Pediatrics Perinatology and Child Health Etiology Surgery Differential diagnosis business |
| Zdroj: | La Pediatria Medica e Chirurgica, Vol 34, Iss 2 (2012) |
| ISSN: | 0391-5387 |
| DOI: | 10.4081/pmc.2012.68 |
| Popis: | The authors describe the case of a newborn and their family with Nonne-Milroy disease (hereditary lymphedema type I), a genetic disease that is usually characterized by lymphedema, that most often affects the lower extremities or less frequently the back of the hands. We discuss etiology, inheritance pattern, differential diagnosis and follow-up. |
| Databáze: | OpenAIRE |
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