Cutaneous Laxity: Causes & Reasons

Possible Causes for Cutaneous Laxity

Pseudoxanthoma elasticum with generalized cutaneous laxity. Arch Dermatol. May 1997;133(5):664-6. [Medline]. 38.Uitto J, Ryhänen L, Abraham PA, Perejda AJ. [hoanmysaigon.com]

Laxity of skin occurs later in life. [web.archive.org]

Cutis laxa, 1074167. 2.Morava E, Lefeber DJ, Urban Z, et al. [hoanmysaigon.com]

Turner Syndrome

laxa: Loose folds of skin, particularly in the neck, are signs in newborns; this is a result of resolving lymphedema and occasionally is observed after infancy See Clinical [emedicine.medscape.com]

Cutis laxa are the loose folds of skin, particularly in the neck, are signs in newborns. [symptoma.com]

[…] aorta, bicuspid aortic valve, and aortic dissection in adulthood Thyroid: Hypothyroidism develops in 10-30% of patients [6] and is often associated with thyroid enlargement Cutis [emedicine.medscape.com]

Cutis Laxa

laxity. [ncbi.nlm.nih.gov]

(ACL) Associated With Plasma Cell Dyscrasias Our patient's cutaneous laxity distribution is consistent with descriptions of prior cases. [jamanetwork.com]

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

Autosomal Recessive Cutis Laxa Type 1A

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

He had the characteristic cutaneous abnormalities described in all the varieties of cutis laxa. [panafrican-med-journal.com]

Acquired cutis laxa is a rare cutaneous manifestation of hematologic malignancy, particularly plasma cell dyscrasias, including multiple myeloma, monoclonal gammopathy of [emedicine.medscape.com]

Congenital Sodium Diarrhea

Please enable JS and disable any ad blocker [cairn.info]

Acquired Cutis Laxa

Six years ago, she observed cutaneous laxity in skin-fold areas and bilateral palpebral ptosis. [scielo.br]

We observed cutaneous laxity, hyper-chromic papules and comedones over the skinfolds, such as the armpits, cervical and inframammary regions ( Figure 2 ). [scielo.br]

(ACL) Associated With Plasma Cell Dyscrasias Our patient's cutaneous laxity distribution is consistent with descriptions of prior cases. [jamanetwork.com]

Autosomal Recessive Cutis Laxa Type 2A

About Library Blog FAQ Testimonials Rare Charities Press Contact Search the Library Other Names: Chalazoderma, Cutaneous laxity, Dermatochalasia, Dermatomegaly, Elastolysis [rareguru.com]

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

laxa type 2A (disorder) synonyms ARCL2A - autosomal recessive cutis laxa type 2A Autosomal recessive cutis laxa type 2A attributes - group3 Finding site Skin structure 39937001 [findacode.com]

FBLN5-Related Cutis Laxa

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet. 2006;78(6):1075–80. [karger.com]

Free Books & Documents Excerpt Clinical characteristics: FBLN5-related cutis laxa is characterized by cutis laxa, early childhood-onset pulmonary emphysema, peripheral pulmonary [pubmed.ncbi.nlm.nih.gov]

Cutis Laxa - Osteoporosis

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

Case Reports Congenital cutis laxa and osteoporosis N O Sakati et al. Am J Dis Child. 1983 May. [pubmed.ncbi.nlm.nih.gov]

EFEMP2-RELATED CUTIS LAXA This disorder is also known as FBLN4-related cutis laxa or autosomal recessive cutis laxa type 1B (ARCL1B). [rarediseases.org]

Autosomal Recessive Cutis Laxa Type 2

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

Discriminative features in three autosomal recessive cutis laxa syndromes: cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica. Int J Mol Sci. 2017;18(3):635. [link.springer.com]

Alternative Names ARCL2A ARCL2 Cutis Laxa with Congenital Disorder of Glycosylation Cutis Laxa with Growth and Developmental Delay Cutis Laxa, Debre Type Cutis Laxa with Bone [cags.org.ae]

Congenital Heart Disease - Radioulnar Synostosis - Mental Retardation

LAXA RN0500 CUTIS LAXA CUTIS LAXA - ANOMALIE GRAVI POLMONARI, GASTROINTESTINALI E DELLE VIE URINARIE RN0500 CUTIS LAXA CUTIS LAXA ACQUISITA RN0500 CUTIS LAXA CUTIS LAXA CONGENITA [malattierare.regione.veneto.it]

RN0500 CUTIS LAXA CUTIS LAXA LEGATA ALL'X RN0500 CUTIS LAXA CUTIS LAXA X-LINKED RN0500 CUTIS LAXA D-HUS CON ANTICORPI ANTI-FATTORE H RGG010 MICROANGIOPATIE TROMBOTICHE La [malattierare.regione.veneto.it]

SINDROMI MALFORMATIVE CONGENITE GRAVI ED INVALIDANTI DEL CUORE E DEI GRANDI VASI CUTE MARMORATA TELEANGECTASICA CONGENITA RN0540 CUTE MARMORATA TELEANGECTASICA CONGENITA CUTIS [malattierare.regione.veneto.it]

Marfanoid Joint Hypermobility Syndrome

Congenital cutis laxa and lysyloxidase deficiency. Congenital cutis laxa and lysyloxidase deficiency. Clin Genet 1997; 51:109–114. [link.springer.com]

Defective protein glycosylation in patients with cutis laxa syndrome. Eur J Hum Genet 2005; 13: 414–421. [link.springer.com]

Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet 2006; 78:1075–1080. [link.springer.com]

Autosomal Recessive Cutis Laxa Type 1B

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

laxa is typified by intense, episodic cutaneous inflammation and recurrent erythematous plaques. [emedicine.medscape.com]

He had the characteristic cutaneous abnormalities described in all the varieties of cutis laxa. [panafrican-med-journal.com]

Autosomal Recessive Cutis Laxa Type 1

The cutaneous laxity that follows is limited to areas of previous inflammation. [emedicine.medscape.com]

Discriminative features in three autosomal recessive cutis laxa syndromes: cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica. Int J Mol Sci. 2017;18(3):635. [link.springer.com]

We present a ten months boy of autosomal recessive cutis laxa type 1 with pulmonary involvement. Keywords: cutis laxa, recessive, sagging skin, type 1. [jmscr.igmpublication.org]

Marfanoid Habitus - Inguinal Hernia - Advanced Bone Age

Congenital cutis laxa and lysyloxidase deficiency. Congenital cutis laxa and lysyloxidase deficiency. Clin Genet 1997; 51:109–114. [link.springer.com]

Defective protein glycosylation in patients with cutis laxa syndrome. Eur J Hum Genet 2005; 13: 414–421. [link.springer.com]

Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet 2006; 78:1075–1080. [link.springer.com]

Autosomal Recessive Cutis Laxa Type 2B

Discriminative features in three autosomal recessive cutis laxa syndromes: cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica. Int J Mol Sci. 2017;18(3):635. [link.springer.com]

Alternative names Autosomal Recessive Cutis Laxa Type 2b Is also known as autosomal recessive cutis laxa type 2, progeroid type, cutis laxa with progeroid features, arcl2, [mendelian.co]

Synonym(s) ARCL2B; Autosomal recessive cutis laxa, type 2B; Cutis laxa, autosomal recessive, type 2B; Cutis laxa with progeroid characteristics; de-Barsy Syndrome B; OMIM: [altmeyers.org]

De Barsey-Moens-Dierckx Syndrome

Cutis laxa Chalazoderma, Elastolysis, Cutaneous laxity, Hypoelastic skin, Loose skin, Hanging skin, Inelastic skin, Dermatomegaly, Lax skin, Generalized elastolysis, Skin [rarediseases.oscar.ncsu.edu]

known as ATP6V0A2-CDG by the new naming system.[5] Alternative names for De Barsy syndrome include corneal clouding-cutis laxa-mental retardation, cutis laxa-growth deficiency [en.wikipedia.org]

Resources - Progeroid syndrome De Barsy type Main name of condition: De Barsy Syndrome Other names or spellings for De Barsy Syndrome : Cutis laxa corneal clouding mental [checkorphan.org]

Autosomal Recessive Cutis Laxa Type 1C

Laxa, Autosomal Recessive, Type Ic, also known as cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities, is related to cutis laxa and ltbp4-related [malacards.org]

Homepage Rare diseases Search Search for a rare disease Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Disease definition A rare, genetic, dermis [orpha.net]

HOW IS CUTIS LAXA INHERITED ? Cutis laxa (CL) is inherited in many different ways, depending on the type of cutis laxa. [cutislaxa.org]

Cutis Laxa-Marfanoid Syndrome

Cutis laxa is usually a genetic disease, but acquired cases have been reported. [rgd.mcw.edu]

Aliases & Classifications for Cutis Laxa, Neonatal, with Marfanoid Phenotype Summaries for Cutis Laxa, Neonatal, with Marfanoid Phenotype MalaCards based summary : Cutis Laxa [malacards.org]

Unlike EDS, joint laxity is not a feature of cutis laxa. [2] Pseudoxanthoma elasticum (PXE) is a unique disorder with predominant cardiovascular and ophthalmologic involvement [bioline.org.br]

X-Linked Recessive Corpus Callosum Dysgenesis

Laxa Type II, Wrinkly Skin Syndrome AR 99.99 55 of 55 ATP6V1A Autosomal Recessive Cutis Laxa Type II, Undetermined Early-Onset Epileptic Encephalopathy AD,AR 99.98 9 of 9 [igenomix.es]

ATP6V1E1 Autosomal Recessive Cutis Laxa Type II AR 100 2 of 2 ATR Familial Cutaneous Telangiectasia And Cancer Syndrome, Seckel Syndrome AD,AR 99.98 39 of 40 B3GALNT2 Muscular [igenomix.es]

Spasticity- Intellectual Disability-Epilepsy Syndrome X,XR,G 81.92 NA of NA ASPM Autosomal Recessive Primary Microcephaly AR 99.74 221 of 222 ATP6V0A2 Autosomal Recessive Cutis [igenomix.es]

Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy

LAXA SINDROME RITARDO DELLA CRESCITA - SORDITA - DEFICIT COGNITIVO RCG031 SINDROMI DA RESISTENZA ALL'ORMONE DELLA CRESCITA SINDROME RITARDO DELLO SVILUPPO-ANOMALIA DEL SISTEMA [malattierare.regione.veneto.it]

GONADICO E/O FENOTIPO SINDROME RHYNS RNG111 ALTRE SINDROMI MALFORMATIVE CONGENITE GRAVI ED INVALIDANTI CON PREVALENTE INTERESSAMENTO DELL'APPARATO VISIVO SINDROME RIN2 RN0500 CUTIS [malattierare.regione.veneto.it]

Elastoderma

CONGENITAL CUTIS LAXA Cutaneous features include pendulous, inelastic skin, with an aged facies. ■ Extracutaneous manifestations may include pulmonary emphysema, aortic aneurysm [slideshare.net]

Elastoderma is a rare cutaneous condition, which clinically presents as an acquired laxity and decreased recoil of skin. [ncbi.nlm.nih.gov]

laxity. [slideshare.net]

Pseudoxanthoma Elasticum

Pseudoxanthoma elasticum (PXE) is an autosomal recessive disorder, characterized by papular skin lesions and cutaneous laxity caused by fragmentation and mineralization of [ncbi.nlm.nih.gov]

Small papular lesions and cutaneous laxity of the neck ("plucked chicken skin") consistent with pseudoxanthoma elasticum. [webeye.ophth.uiowa.edu]

laxity) and/or a positive biopsy of the skin. [symptoma.com]

Occipital Horn Syndrome

Diagnosis of cutis laxa. [malattierare.regione.veneto.it]

Arch-Ophthalmol. 2001 Feb; 119(2): 285-8 Braakenburg,-A; Nicolai,-J-P Bilateral eyelid edema: cutis laxa or blepharochalasis? [malattierare.regione.veneto.it]

Matrix-Biol. 2000 Nov; 19(6): 471-80 Ma'luf,-R-N; Ghazi,-N; Ghanim,-M-N; Tawal,-A-N Involution type of entropion in a child with cutis laxa. [malattierare.regione.veneto.it]

Lenz-Majewski Syndrome

Other clinical features include dysplastic teeth, skin hypoplasia joint laxity, choanal atresia, short digits, and partial syndactyly. [accesspediatrics.mhmedical.com]

Other clinical features include dysplastic teeth, skin hypoplasia, joint laxity, choanal atresia, short digits, and partial syndactyly. [accessanesthesiology.mhmedical.com]

From Wikidata Jump to navigation Jump to search Lenz-Majewski hyperostotic dwarfism is an extremely rare syndrome associating dwarfism, characteristic facial appearance, cutis [wikidata.org]

Autosomal Recessive Mental Retardation Type 45

Diagnosis of cutis laxa. [malattierare.regione.veneto.it]

Arch-Ophthalmol. 2001 Feb; 119(2): 285-8 Braakenburg,-A; Nicolai,-J-P Bilateral eyelid edema: cutis laxa or blepharochalasis? [malattierare.regione.veneto.it]

Matrix-Biol. 2000 Nov; 19(6): 471-80 Ma'luf,-R-N; Ghazi,-N; Ghanim,-M-N; Tawal,-A-N Involution type of entropion in a child with cutis laxa. [malattierare.regione.veneto.it]

Ehlers-Danlos Syndrome Arthrochalasia Type 2

Laxa, And Scoliosis, RIN2 Syndrome AR 99.60% 4 of 4 RIPK1 Autoinflammation With Episodic Fever And Lymphadenopathy, Immunodeficiency AD,AR 98.03% 12 of 14 RPGR Primary Ciliary [igenomix.es]

Lymphopenia, Neutrophil Immunodeficiency Syndrome AD,AR 100% 5 of 5 RASGRP1 Autoimmune Lymphoproliferative Syndrome, Immunodeficiency AR 98.41% 8 of 9 RIN2 Macrocephaly, Alopecia, Cutis [igenomix.es]

Corneal Dystrophy - Pigmentary Anomaly - Malabsorption

LAXA ITTIOSI TIPO HARL Page 18 and 19: RN1210 SMITH-MAGENIS, SINDROME DI R Page 20 and 21: RN1790 RN1800 RN1810 DISPLASIA NEUR Page 22 and 23: 278 Page 24 and 25: 280 Page [yumpu.com]

LAXA RN0510 INCONTINENTIA PIGMENTI RN0520 XERODERMA PIGMENTOSO RN0530 CHERATOSI FOLLICOLARE ACUMINATA RN0540 CUTE MARMOREA TELEANGECTASICA CONGENITA RN0550 DARIER MALATTIA [amareonlus.it]

LAXA (RN0510) INCONTINENTIA PIGMENTI (RN0520) XERODERMA PIGMENTOSO (RN0530) CHERATOSI FOLLICOLARE ACUMINATA (RN0540) CUTE MARMORATA TELEANGECTASICA CONGENITA (RN0550) DARIER [malattierare.toscana.it]

Lymphoplasmacytic Lymphoma Without IgM Production

Laxa Turk J Haematol 2020 [ Links ] 28 Nelson CA, Zhong CS, Hashemi DA, Ashchyan HJ, Brown-Joel Z, Noe MH, et al A Multicenter Cross-Sectional Study and Systematic Review [scielo.cl]

Mid-Dermal Elastolysis

Diagnosis of cutis laxa. [malattierare.regione.veneto.it]

March 1988; 13: 38b Google Scholar Delacretaz J Perroud H Vulliemin JF Cutis laxa acquise. [jaad.org]

Int J Dermatol 25: 171–173 PubMed Google Scholar Delacrétaz J, Perroud H, Vulliemin JF (1977) Cutis laxa acquisé. [link.springer.com]