Ectodermal Dysplasia Associated with Sickle Cell Disease
Ectodermal dysplasia and sickle cell anaemia are inherited disorders that affect, respectively, the tissues derived from the embryonic ectoderm and the production of erythrocytes by the bone marrow. The simultaneous occurrence of both disorders is extremely rare. This is a case of both ectodermal dy...
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Hindawi Limited,
2014-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_2d2e6d2ef6a647ec96e16ca37e504de3 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Luiz Evaristo Ricci Volpato |e author |
700 | 1 | 0 | |a Maria Carmen Palma Faria Volpato |e author |
700 | 1 | 0 | |a Artur Aburad de Carvalhosa |e author |
700 | 1 | 0 | |a Vinicius Canavarros Palma |e author |
700 | 1 | 0 | |a Álvaro Henrique Borges |e author |
245 | 0 | 0 | |a Ectodermal Dysplasia Associated with Sickle Cell Disease |
260 | |b Hindawi Limited, |c 2014-01-01T00:00:00Z. | ||
500 | |a 2090-6447 | ||
500 | |a 2090-6455 | ||
500 | |a 10.1155/2014/314391 | ||
520 | |a Ectodermal dysplasia and sickle cell anaemia are inherited disorders that affect, respectively, the tissues derived from the embryonic ectoderm and the production of erythrocytes by the bone marrow. The simultaneous occurrence of both disorders is extremely rare. This is a case of both ectodermal dysplasia and sickle cell anaemia reported in a 6-year-old. The patient had been diagnosed with sickle cell anaemia for only six months when he sought treatment presenting with the following: hypotrichosis, dry skin, periocular hyperpigmentation, protruding lips, hypodontia, and morphologically altered teeth. The clinical features combined with his medical history led to the diagnosis of ectodermal dysplasia. Dentists should be prepared to recognise patterns that escape normality to aid in the diagnosis of systemic changes, even in patients with other previous diagnoses. | ||
546 | |a EN | ||
690 | |a Dentistry | ||
690 | |a RK1-715 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Case Reports in Dentistry, Vol 2014 (2014) | |
787 | 0 | |n http://dx.doi.org/10.1155/2014/314391 | |
787 | 0 | |n https://doaj.org/toc/2090-6447 | |
787 | 0 | |n https://doaj.org/toc/2090-6455 | |
856 | 4 | 1 | |u https://doaj.org/article/2d2e6d2ef6a647ec96e16ca37e504de3 |z Connect to this object online. |