Llwytho...
Goltz Syndrome: A Newborn with Ectrodactyly and Skin Lesions
Goltz syndrome or Focal Dermal Hypoplasia is a rare multisystem disorder, involving all the three germ cell layers. The disease is thought to be inherited in X-linked dominant fashion with heterogeneous mutations of the PORCN gene at Xp11.23 locus. Majority of the cases are sporadic, mainly due to p...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Indian J Dermatol |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Medknow Publications & Media Pvt Ltd
2015
|
| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4372956/ https://ncbi.nlm.nih.gov/pubmed/25814752 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.152608 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|