Limb–mammary syndrome

{{Infobox medical condition (new)

| name = Limb–mammary syndrome

| synonyms = LMS{{cite web |title=OMIM Entry - # 603543 - LIMB-MAMMARY SYNDROME; LMS |url=https://omim.org/entry/603543 |website=omim.org |access-date=27 April 2019}}

| 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

| pronounce =

| field = Medical genetics

| geneReviewsID =

| symptoms =

| complications =

| onset =

| duration =

| types =

| causes =

| risks =

| diagnosis =

| differential =

| prevention =

| treatment =

| medication =

| prognosis =

| frequency =

| deaths =

}}

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

{{reflist}}

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]