Keratoderma climactericum

{{Infobox medical condition (new)

| name =

| synonym = Climacteric keratoderma, Haxthausen's disease,{{cite journal | pmid = 2943612 | volume=172 | issue=5 | title=Keratoderma climactericum (Haxthausen's disease): clinical signs, laboratory findings and etretinate treatment in 10 patients | year=1986 | vauthors=Deschamps P, Leroy D, Pedailles S, Mandard JC | journal=Dermatologica | pages=258–62 | doi=10.1159/000249351}} and Acquired plantar keratoderma,{{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 |pages=205 |isbn=978-1-4160-2999-1 }}

| image =

| image_size =

| alt =

| caption =

| pronounce =

| specialty = Dermatology

| symptoms =

| complications =

| onset =

| duration =

| types =

| causes =

| risks =

| diagnosis =

| differential =

| prevention =

| treatment =

| medication =

| prognosis =

| frequency =

| deaths =

}}

Keratoderma climactericum, also known as climacteric keratoderma, Haxthausen's disease, or acquired plantar keratoderma, is a skin condition characterized by hyperkeratosis of the palms and soles beginning at about the time of menopause.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}.{{rp|213}}Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. {{ISBN|0-07-138076-0}}.