Hypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentation
The ectodermal dysplasias are a heterogenous group of diseases, which have one or more anomalies of the hair, teeth, nails, and sweat glands. Hypohidrotic ectodermal dysplasia (HED) is the most common type and is usually transmitted as an X-linked recessive trait. It is characterized by classical tr...
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| Format: | Book |
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Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | doaj_13ccb6d5c7104e9985fe901bafd5b2ad | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Manisha Goyal |e author |
| 700 | 1 | 0 | |a Gaurav Pradhan |e author |
| 700 | 1 | 0 | |a Sunita Gupta |e author |
| 700 | 1 | 0 | |a Seema Kapoor |e author |
| 245 | 0 | 0 | |a Hypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentation |
| 260 | |b Wolters Kluwer Medknow Publications, |c 2015-01-01T00:00:00Z. | ||
| 500 | |a 0976-237X | ||
| 500 | |a 0976-2361 | ||
| 500 | |a 10.4103/0976-237X.149304 | ||
| 520 | |a The ectodermal dysplasias are a heterogenous group of diseases, which have one or more anomalies of the hair, teeth, nails, and sweat glands. Hypohidrotic ectodermal dysplasia (HED) is the most common type and is usually transmitted as an X-linked recessive trait. It is characterized by classical triad of hypotrichosis, anhidrosis/hypohidrosis, and hypodontia/anodontia. Here, we describe an Indian boy affected with HED and rare features including ankylosis of temporomandibular joint and cleft palate. | ||
| 546 | |a EN | ||
| 690 | |a Cleft palate | ||
| 690 | |a hypodontia | ||
| 690 | |a hypohydrosis | ||
| 690 | |a Dentistry | ||
| 690 | |a RK1-715 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Contemporary Clinical Dentistry, Vol 6, Iss 1, Pp 110-112 (2015) | |
| 787 | 0 | |n http://www.contempclindent.org/article.asp?issn=0976-237X;year=2015;volume=6;issue=1;spage=110;epage=112;aulast=Goyal | |
| 787 | 0 | |n https://doaj.org/toc/0976-237X | |
| 787 | 0 | |n https://doaj.org/toc/0976-2361 | |
| 856 | 4 | 1 | |u https://doaj.org/article/13ccb6d5c7104e9985fe901bafd5b2ad |z Connect to this object online. |