Limb–mammary syndrome
{{Infobox medical condition (new)
| name = Limb–mammary syndrome
| image = Main_droite_1_mois.jpg
| alt = colour photograph of a hand of a patient with Limb–mammary syndrome. Two out of 3 fingers are present with 2 fingers fused
| caption = hand of patient with Limb–mammary syndrome
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| field = Medical genetics
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Limb–mammary syndrome is a cutaneous condition characterized by p63 mutations.{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 }}
See also
References
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Further reading
- [https://www.ncbi.nlm.nih.gov/books/NBK43797/ GeneReviews/NCBI/NIH/UW entry on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate Syndrome or AEC Syndrome, Hay-Wells Syndrome. Includes: Rapp–Hodgkin Syndrome]
External links
{{Medical resources
| DiseasesDB = 32743
| ICD10 = {{ICD10|Q|82|4|q|82}}
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| OMIM = 603543
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| SNOMED CT = 721972001
| Orphanet = 69085
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- [https://www.ncbi.nlm.nih.gov/omim/106260,603273,106260,603273 OMIM entries on AEC]
{{Transcription factor/coregulator deficiencies}}
{{DEFAULTSORT:Limb-mammary syndrome}}
Category:Cutaneous congenital anomalies
Category:Syndromes affecting the skin
{{Genodermatoses-stub}}