Search results for "Genitalia"

showing 5 items of 155 documents

High prevalence and little awareness in patients with chronic inflammatory skin diseases and genital involvement.

2020

Background Genital involvement in patients with chronic inflammatory skin diseases is frequent, yet insufficiently acknowledged. Objective To evaluate the prevalence of genital symptoms in psoriasis and chronic urticaria patients, effects on quality of life, physician-patient relations and disease management. Patients and methods 100 patients with psoriasis and 100 with chronic urticaria from our outpatient clinic, as well as 50 healthy controls were included. Data was collected using questionnaires developed by dermatological experts. Results Out of 250 subjects, 74 % had already experienced genital symptoms - 70 % of psoriasis patients and 58 % of urticaria patients. Seven out of ten even…

medicine.medical_specialtyHigh prevalenceUrticariabusiness.industry610 MedizinDermatologymedicine.diseaseDermatologyQuality of lifePsoriasis610 Medical sciencesChronic DiseasemedicinePrevalenceQuality of LifeOutpatient clinicHumansPsoriasisSex organIn patientGenitaliaDisease management (health)skin and connective tissue diseasesbusinessChronic urticariaJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDGReferences
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Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder.

2009

We report on a 7-year-old girl with unequivocal features of Barber-Say syndrome (BSS): generalized hypertrichosis especially at the back, dry lax skin, macrostomia, thin lips, cup-shaped ears, bulbous nose, hypoplastic nipples, and abnormal external genitalia. She also demonstrated conductive hearing impairment and microblepharon. BSS has been reported with ectropion (not present in our patient), but ablepharon and microblepharon (i.e., absent or hypoplastic eyelids) have always been considered as hallmarks of ablepharon macrostomia syndrome (AMS). This is the first report of microblepharon in BSS. Other authors have discussed that BSS and AMS could possibly represent one syndrome, and our …

medicine.medical_specialtyHypertrichosisSkin DiseasesConductive hearing impairmentDiagnosis DifferentialAblepharonAblepharon macrostomia syndromeGeneticsmedicineHumansAbnormalities MultipleChildGenetics (clinical)Macrostomiabiologybusiness.industryEctropionEyelidsGeneralized hypertrichosisSyndromemedicine.diseaseMicroblepharonbiology.organism_classificationDermatologyAbnormal external genitaliaMacrostomiaFemalesense organsbusinessAmerican journal of medical genetics. Part A
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Technical Detail on Nerve Coaptation in Phalloplasty: Use of Fibrin Glue Instead of Sutures.

2019

medicine.medical_specialtySuturesComputer scienceUrologyEndocrinology Diabetes and MetabolismObstetrics and GynecologyFibrin Tissue AdhesiveSurgeryPsychiatry and Mental healthEndocrinologyReproductive MedicinemedicineSex Reassignment SurgeryTissue AdhesivesPhalloplastyGenitaliaFibrin glueSexual medicine reviews
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The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

1983

We report 17 cases of the campomelic syndrome (CS) and a follow-up of one of the original patients of Maroteaux et al who is now 17 years old. Our review is based on 97 patients, including our own. An infant with the CS presents at birth with spectacularly short and bowed femora and tibiae. The initial chest radiograph confirms the diagnosis by demonstrating extremely small bladeless scapulae and hypoplastic pedicles of many thoracic vertebrae. Ossification of the sternal segments, pubis, talus, and knee epiphyses is also retarded. Usually the hips are dislocated and talipes equinovarus deformities are present. There is a small chondrocranium and a disproportionately large neurocranium. The…

musculoskeletal diseasesMaleAdolescentH-Y AntigenRespiratory SystemBone and BonesmedicineHumansAbnormalities MultipleGenitaliaHydronephrosisGenetics (clinical)Respiratory Distress Syndrome NewbornRespiratory distressmedicine.diagnostic_testOssificationbusiness.industryInfant NewbornAnatomySyndromemusculoskeletal systemmedicine.diseaseRenal hypoplasiaHypotoniaCampomelic dysplasiamedicine.anatomical_structureCartilageThoracic vertebraeFemalemedicine.symptomChest radiographbusinessAmerican journal of medical genetics
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Macroscytus raunoi, a new burrower bug species from Papua New Guinea (Hemiptera: Heteroptera: Cydnidae: Cydninae)

2016

Abstract Macroscytus raunoi, a new species of the genus Macroscytus Fieber, 1860, is described from the Morobe Province on the northern coast of Papua New Guinea. The new species is similar in its morphological characters to Australian M. arnhemicus J. A. Lis, 1999. Differences in morphology and male genitalia which enable separation of both species are provided.

new species0106 biological sciencesMacroscytusbiologyCydninaeMale genitaliaHeteroptera010607 zoologyNew guineaMorphology (biology)biology.organism_classification010603 evolutionary biology01 natural sciencesHemipteraAustralian RegionMacroscytusGenusInsect ScienceBotanyCydnidaeEntomologica Americana
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