Acrogeria: Causes & Reasons

Possible Causes for Acrogeria

The skin on the extremities appears prematurely aged, hence the term acrogeria, and the subcutaneous veins are highly visible. [ncbi.nlm.nih.gov]

Pope FM, Narcisi P, Nicholls AC, Germain DP, Pals G, Richards AJ: COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture. [ojrd.biomedcentral.com]

Patients may also have acrogeria, which is a prematurely aged appearance of the extremities (see photo below). [forgottendiseases.org]

Ehlers-Danlos Syndrome

A slightly extensible, thin and translucent skin, associated with dysmorphic facies, acrogeria, multiple ecchymoses, hypermobility of the small joints, dorsal kyphosis, genu [ncbi.nlm.nih.gov]

[…] syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria [orpha.net]

Acromelanosis

Causes of Irregular hyperpigmentation Some of the causes of the condition may include: Causes of Irregular Hyperpigmentation : Acrogeria Acromelanosis Albinism-Deafness Syndrome [familydiagnosis.com]

Some causes may include: 1 Causes of Irregular Hyperpigmentation : Acrogeria Acromelanosis Albinism-Deafness Syndrome Alkaptonuria Autosomal Dominant Hypocalcemia Bannayan-Riley-Ruvalcaba [familydiagnosis.com]

Download as PDF, TXT or read online Acrodermatitis enteropática Acrodermatitis papulosa infantil Acrodinia Acroesclerosis Acrogeria Acromelanosis Acromelanosis. [ucypunireqy.cf]

Premature Aging Type Okamoto

Acrogeria Other names Acrogeria, Gottron type, Gottron's syndrome[1] Collagen(which is below normal/damaged in this condition)[2] Specialty Dermatology Acrogeria (Gottron's [en.wikipedia.org]

[…] share one's experience with acrogeria [en.wikipedia.org]

External links[edit] Classification D OMIM: 201200 MeSH: C538187 Familial acrogeria in a brother and sister A case of acrogeria - A rare aging syndrome Discussion forum to [en.wikipedia.org]

Elastosis perforans serpiginosa

Down syndrome, osteogenesis imperfecta, acrogeria, Ehlers-Danlos syndrome type IV, Marfan syndrome, pseudoxanthoma elasticum, Rothmund-Thomson syndrome, and scleroderma have [ncbi.nlm.nih.gov]

These include Marfan syndrome, osteogenesis imperfecta, cutis laxa, acrogeria, Ehlers-Danlos syndrome, Rothmund-Thomson syndroma and Down syndrome. [neurologyadvisor.com]

[…] conditions and connective tissue disorders including Down's syndrome, Ehlers-Danlos syndrome type IV (vascular type), osteogenesis imperfecta, scleroderma, diabetes mellitus, acrogeria [xpertdox.com]

Ehlers-Danlos-Syndrome Type 10

The skin on the extremities appears prematurely aged, hence the term acrogeria, and the subcutaneous veins are highly visible. [ojrd.biomedcentral.com]

COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture. [ncbi.nlm.nih.gov]

[…] noticeable on the chest/abdomen) Easy bruising (spontaneous or with minimal trauma) Characteristic facial appearance (thin lips and philtrum, small chin, thin nose, large eyes) Acrogeria [uwcpdx.org]

Ehlers-Danlos Syndrom Classic Type 2

The skin on the extremities appears prematurely aged, hence the term acrogeria, and the subcutaneous veins are highly visible. [ojrd.biomedcentral.com]

[…] intestinal/uterine fragility or rupture which can be life threatening Extensive bruising Other characteristics Normal scar formation May be increased incidence of stroke Acrogeria [en.wikibooks.org]

Acroosteolysis-Keloid-Like Lesions-Premature Aging Syndrome

The most widely studied of thesegenodermatoses are progeria infantum (HutchinsonGilford syndrome), Werner syndrome (progeria adulto-rum), acrogeria (Gottron type), acrometageria [documents.tips]

[…] low C3, presence of C3-nephritic factor, no insulin resistance; presence of other autoimmune diseases J Clin Endocrinol Metab 85:1776–1782, 2000 Acrocephalopolysyndactyly Acrogeria [yumpu.com]

[…] deafness hand syndrome Myoclonus hereditary progressive distal muscular atrophy Steinfeld syndrome Cardiomyopathy dilated with woolly hair and keratoderma De Barsy syndrome Acrogeria [checkrare.com]

Ehlers-Danlos Syndrome Hypermobility Type

IV, también conocido como síndrome de Ehlers-Danlos (SED) de tipo vascular, es un trastorno hereditario del tejido conectivo definido por rasgos faciales característicos (acrogeria [femexer.org]

Ehlers-Danlos Syndrome Classic-Like Type 1

The skin on the extremities appears prematurely aged, hence the term acrogeria, and the subcutaneous veins are highly visible. [ojrd.biomedcentral.com]

Clinical diagnosis of vascular Ehlers-Danlos syndrome is based on four criteria: a characteristic facial aspect (acrogeria) in most patients, thin and translucent skin with [syndrome.medicclub.info]

Short Stature - Amelogenesis Imperfecta - Skeletal Dysplasia with Scoliosis

Stanescu Type, Spondylometaphyseal Dysplasia ‘Corner Fracture’ Type, Spondyloperipheral Dysplasia, Short Ulna Syndrome, Stickler Syndrome Type 1 AD,MU 100% 583 of 583 COL3A1 Acrogeria [igenomix.es]

Acrogeria

Acrogeria Other names Acrogeria, Gottron type, Gottron's syndrome[1] Fibers of Collagen Type I - TEM Specialty Dermatology Acrogeria (Gottron's syndrome) is a skin condition [en.wikipedia.org]

External links[edit] Familial acrogeria in a brother and sister [en.wikipedia.org]

"Acrogeria of the Gottron type in a mother and son". Eur J Dermatol. 10 (1): 36–40. PMID 10694296. ^ Pope FM, Narcisi P, Nicholls AC, et al. (1996). [en.wikipedia.org]

Ehlers-Danlos Syndrome Classic-Like Type 2

Ehlers-Danlos syndrome classic-like-2 is characterized by severe joint and skin laxity, osteoporosis involving the hips and spine, osteoarthritis, soft redundant skin that can be acrogeria-like [malacards.org]

In addition, skin of the hands and feet may appear prematurely aged (acrogeria). vEDS is particularly associated with arterial dissection and rupture, intestinal perforation [rarediseases.org]

EDSCLL2 patients show severe joint and skin laxity, osteoporosis affecting the hips and spine, osteoarthritis, soft redundant skin that can be acrogeria-like, delayed wound [malacards.org]

Ehlers-Danlos Syndrome Type Friedman-Harrod

[…] bruising, hypermobility mainly of the distal joints, skin hyperextensibility and fragility, abnormal scarring, recurrent infections, hernias, marfanoid facial features, acrogeria [ncbi.nlm.nih.gov]

Progeroid Syndrome Type Petty

In 1992 Greally et al. [3] described a boy with features of both acrogeria and metageria, and hypothesized that acrogeria and metageria are part of the phenotypic spectrum [plasticsurgerykey.com]

Syndrome ; Werner Syndrome Other names Hutchinson- Gilford Syndrome; Syndrome, Hutchinson- Gilford; Hutchinson Gilford Syndrome Substance CAS Registry & name Categories Source Acrogeria [reference.md]

Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria [paperity.org]

Cataract - Skeletal Anomalies

Skeletal Dysplasia - Orofacial Anomalies

Mandibuloacral Dysplasia with Type B Lipodystrophy

The family reported as an example of acrogeria by Rezai-Delui et al., (1999) where four individuals from three inbred sibships were affected, probably had mandibulo-acral [fdna.health]

Anonychia with Flexural Pigmentation

Localized Hyperpigmentation Anonychia with Flexural Pigmentation Incontinentia Pigmenti Periorbital Hyperpigmentation 48 Genetic Epidermal Syndromes: Disorders of Aging Acrogeria [homepage.vghtpe.gov.tw]

Acrogeria ( Nancy Burton Esterly, Eulalia Baselga, Peter M. H.Chan, & Beth A. Drolet ). Metageria ( Nancy Burton Esterly, Eulalia Baselga, Peter M. H.Chan, & Beth A. [amazon.it]

Infants with congenital disorders that have a progressive phenotype, such as acrogeria or dyskeratosis congenita, can have onychoatrophy as well. [clinicalgate.com]

Ehlers-Danlos Syndrome Kyphoscoliotic Type 1

Vascular type is associated by thin, translucent skin that is extremely fragile and bruises easily, acrogeria, characteristic facial features and pneumothorax. [xpertdox.com]

( Hyperextensible skin, sagging of skin, acrogeria( older appearance), cigar shaped scars,keloid formation) Mitral Prolapse and Aortic Regurgitation cannot be ruled out [forums.studentdoctor.net]

Other manifestations that may be found in include: acrogeria; early onset varicose veins; arteriovenous, carotid-cavernous fistula; pneumothorax/pneumohemothorax; gingival [ehlersdanlos.ca]

Dermatosparaxis

Other common features include tendon and/or muscle rupture; acrogeria (premature aging of the skin of the hands and feet); pneumothorax (collapse of a lung). [marfan.org]

[…] lobeless ears joint hypermobility is present, but generally confined to the small joints (fingers, toes) other common features include club foot; tendon and/or muscle rupture; acrogeria [gpnotebook.com]

Ehlers-Danlos Syndrome Arthrochalasia Type

( Hyperextensible skin, sagging of skin, acrogeria( older appearance), cigar shaped scars,keloid formation) Mitral Prolapse and Aortic Regurgitation cannot be ruled out [forums.studentdoctor.net]

The skin on the extremities appears prematurely aged, hence the term acrogeria, and the subcutaneous veins are highly visible. [ojrd.biomedcentral.com]

Ehlers-Danlos Syndrome Periodontitis Type 1

Acrogeria-an aged appearance in the extremities, particularly the hands-was apparent. [ijo.in]

Features of pEDS Periodontitis Lack of attached gingiva Protibial plaques Pretibial hyperpigmentation Acrogeria Skin and gum fragility Dystrophic scarring Distal joint hypermobility [creative-biolabs.com]

Familial Joint Laxity

Facial dysmorphy – acrogeria is the presence of prominent cheekbones and sunken cheeks. [journals.viamedica.pl]

The skin on the extremities appears prematurely aged, hence the term acrogeria, and the subcutaneous veins are highly visible. [ojrd.biomedcentral.com]

Acrogeria (an aged appearance to the extremities, particularly the hands); Hypermobility of small joints; Tendon/muscle rupture; Early-onset varicose veins; Arteriovenous [ibis-birthdefects.org]

Anophthalmia or Microphthalmia - Esophageal Atresia Syndrome

Download as PDF, TXT or read online Acrodermatitis enteropática Acrodermatitis papulosa infantil Acrodinia Acroesclerosis Acrogeria Acromelanosis Acromelanosis. [rudosubyyoq.tk]

Acquired acromelanosis has been reported to be induced by as PDF, TXT or read online Acrodermatitis enteropática Acrodermatitis papulosa infantil Acrodinia Acroesclerosis Acrogeria [pejugabaq.tk]

Ehlers-Danlos Syndrome Spondylodysplastic Type 3

COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture. [ncbi.nlm.nih.gov]

[…] collagen) Incidence: 1 in 15,000--20,000 • Purpura • Massive internal bleeding • Spontaneous bowel rupture • Peripartum uterine hemorrhage Vascular EDS Associated Features • Acrogeria [studyslide.com]

Acrogeria: A prematurely aged appearance particularly to the hands and feet due to thin wrinkled skin is sometimes seen. [adc.bmj.com]

Thanatophoric Dysplasia Type 2

Congenital Disorder of Glycosylation Type 1G

[…] diseases, like HYPERTRYPTOPHANEMIA; HYPTRP CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34 ACROGERIA [mendelian.co]

Polymicrogyria - Ehlers-Danlos Syndrome Type 4

[…] pain Positive family history Vascular AD COL3A1 Thin, translucent skin Arterial/intestinal/uterine fragility or rupture Extensive bruising Characteristic facial appearance Acrogeria [ncbi.nlm.nih.gov]

[…] volar side of lower arm) Smooth, velvety skin Wide, atrophic scars Molluscoid pseudotumors Subcutaneous feroids Thin, translucent skin, characteristic facial appearance, and acrogeria [ncbi.nlm.nih.gov]

Thanatophoric Dysplasia Type 1