"Webbed neck"

Surgical correction of the webbed neck: an alternative lateral approach The webbed neck deformity or pterygium colli is the number one symptom of the Turner syndrome that leads the patient to consult a doctor. Various but rare surgical approaches have been described to correct this deformity. We reviewed our experience with the surgical correction of the pterygium colli. Through five clinical

Mehri Turki Webbed Neck Classification This study aims to identify all types of congenital neck deformities called " webbed neck ". Through a literature survey, the researcher selected 27 articles describing the surgical treatment of the webbed neck, but without considering the varieties of this deformity. For this reason, the researcher studied all the reported cases from which she developed a classification containing 4 types of webbed necks allowing the use of the most suitable technique to enhance the surgical outcomes. Through a literature survey of 27 selected articles (from PubMed database and clarivate web of science). The publication years ranged from 1937 to 2020 and the number of patients reported to have undergone surgery was 78 patients. The webbed neck is a noticeable congenital

Mehri Turki Surgical Technique of the Webbed Neck The webbed neck is one of the conspicuous deformities of Turner syndrome that presents a surgical challenge. Despite the availability of surgical techniques, surgical outcomes are not always acceptable and recurrence occurs. Mehri Turki performed a surgical technique based on a latéral cervical approach allowing direct visual control to manage the fibrotic band. It provides a high level of visual control so that vulnerable anatomic structures are easily protected. Five girls between 17 and 19 years old, with Turner syndrome, had a webbed neck (pterygium colli) with low and laterally displaced nuchal hairline. The surgical technique aims to correct neck contour and hairline placement while concealing cervical scars. Thus, Preoperative drawing

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Webbed Neck Webbed Neck * Versions * Standard Desktop * Legacy Desktop * Mobile Web * Iphone/Ipad App * * Help Toggle navigation * * Home * Books: A to N * Cardiovascular Medicine * Dentistry * Dermatology * Emergency Medicine * Endocrinology * Gastroenterology * Geriatric Medicine * Gynecology to Palliative Care * * Administration * Patient Satisfaction * Documentation 4 * * advertisement * Home * Neonatology Book * Otolaryngology Chapter * Webbed Neck Webbed Neck Aka: Webbed Neck, Pterygium Colli Deformity, Neck Webbing Neonatology Otolaryngology Chapter * Choanal * Choanal Atresia * Cleft * Cleft Lip * Congenital

occur withnormal XX and XY karyotypes and a variety of abnormal kar-yotypes, most commonly 45, X (Turner syndrome), in whichoocyte loss is accelerated Add after 18 weeks in utero(29,30). Turner syndrome is often diagnosed in early child-hood because of the well-known phenotypic characteristics(short stature, webbed neck, and low hairline), and therefore,many patients do not present for assessment . Philadelphia: WB Saunders; 1996.28.Manuel M, Katayama PK, Jones HW Jr. The age of occurrence of gonadaltumors in intersex patients with a Y chromosome. Am J Obstet Gynecol1976;124:293–300.29.Turner HH. A syndrome of infantilism, congenital webbed neck, and cubitusvalgus. Endocrinology 1938;23:566–74.30.Turner’s syndrome. West J Med 1982;137:32–44.31.Toledo SP, Brunner HG, Kraaij R, Post M, Dahia PL

, most commonly 45, X (Turner syndrome), in which oocyte loss is accelerated Add after 18 weeks in utero (29, 30). Turner syndrome is often diagnosed in early childhood because of the well-known phenotypic characteristics (short stature, webbed neck, and low hairline), and therefore, many patients do not present for assessment of primary amenorrhea. Uncommon causes of ovarian failure include FSH Endocrinol (Oxf) 2012;76:894–8.Reid RL. Amenorrhea. In: Copeland LJ, editor. Textbook of gynecology. 2nd ed. Philadelphia: WB Saunders; 1996.Manuel M, Katayama PK, Jones HW Jr. The age of occurrence of gonadal tumors in intersex patients with a Y chromosome. Am J Obstet Gynecol 1976;124:293–300.Turner HH. A syndrome of infantilism, congenital webbed neck, and cubitus valgus. Endocrinology 1938;23:566–74

features such as short stature and premature ovarian failure.[1]Ullrich O. Uber typische Kombinationsbilder multipler Abartungen. Z. Kinderheilk. 1930;49:271-276.[2]Turner HH. A syndrome of infantilism, congenital webbed neck, and cubitus valgus. Endocrinology. 1938;23:566-574.[3]Gravholt CH, Andersen NH, Conway GS, et al. Clinical practice guidelines for the care of girls and women with Turner syndrome : proceedings from the 2016 Cincinnati International Turner Syndrome Meeting. Eur J Endocrinol. 2017 Sep;177(3):G1-G70.https://www.doi.org/10.1530/EJE-17-0430http://www.ncbi.nlm.nih.gov/pubmed/28705803?tool=bestpractice.comHistory and examKey diagnostic factors * poor growth * short stature * delayed/absent pubertal development * primary amenorrhoea * congenital heart defects * skeletal abnormalities * webbed

Neck apposition is a key factor for aneurysm occlusion after Woven EndoBridge device embolization. Sealing of the aneurysm neck with a Woven EndoBridge (WEB) device is recommended for disrupting the blood flow inside the aneurysm. This study investigates the relationship between WEB neck apposition and aneurysm occlusion rates. Aneurysms treated with a WEB from March 2017 to May 2022 at a single center were included. WEB neck apposition (poor/good) and WEB protrusion (yes/no) were evaluated on post-detachment high resolution cone beam CT images. Angiographic occlusion was assessed with the Bicêtre Occlusion Scale score (BOSS). Univariate and multivariable analysis tested the association between neck apposition and occlusion rates. The study included 159 aneurysms in 141 patients (mean age 55.8

of Noonan syndrome (NS) with double IVC who presented with macrohematuria and proteinuria. The patient was a 23-year-old man, who had been diagnosed with NS due to RIT1 mutation, after showing foamy macrohematuria 3 weeks previously. A physical examination revealed low-set ears and a webbed neck. A urinalysis showed hematuria and proteinuria, and urinary sediments showed more than 100 isomorphic red blood

, webbed neck, a grade 2/6 systolic murmur at lower left sternal area and bilateral absent flexion creases of dig were observed. After treatment, the size and function of the heart recovered to normal at age 13 months. However, the ventricular septum and LV wall were thicker than normal values. Then, the diagnosis was revised to hypertrophic cardiomyopathy(HCM) and suspected congenital malformation of them transitioned to HCM at the disease progression stage. Eight patients presented with HCM at early stage of disease. Nine patients initially exhibited a mixed phenotype of DCM and HCM, and 6 of them eventually progressed to HCM. Electrocardiogram showed prolonged QT interval. Extracardiac features included short stature, special face, cleft palate, webbed neck, joint contracture, and scoliosis

GH Responsiveness in Children With Noonan Syndrome Compared to Turner Syndrome. Despite different genetic background, Noonan syndrome (NS) shares similar phenotype features to Turner syndrome (TS) such as short stature, webbed neck and congenital heart defects. TS is an entity with decreased growth hormone (GH) responsiveness. Whether this is found in NS is debated. Data were retrieved from

Pterygium colli (webbed neck) 25 Thorax Broad chest (shield chest) 30 Inverted nipples 5

THIS ARTICLEEpidemiologyClinical featuresGenetic counsellingDifferential diagnosisDiagnosisManagementPrognosisNoonan syndrome (NS) is a common genetic disorder with multiple congenital abnormalities. It is characterised by congenital heart disease, short stature, a broad and webbed neck, sternal deformity, variable degree of developmental delay, cryptorchidism, increased bleeding tendency and characteristic facial features

and are called streak gonads. In females, the most common form of gonadal dysgenesis is Turner syndrome (45,X), in which gonadotropin levels, especially the FSH levels, are high during early childhood and after age 9-10 years.Additional anomalies associated with Turner syndrome include short stature, webbed neck, coarctation of the aorta (10%), renal abnormalities (50%), hypertension, pigmented nevi, short

skin advancement.Turner SyndromeThis occurs in females. A webbed neck, infantilism, and cubitus valgus are observed. Another term for this condition is pterygium colli. Patients have ovarian agenesis and dwarfism. These girls have only 44 autosomes and one sex chromosome, the X-O.The findings are dwarfism, webbed neck, low hairline, epicanthal folds, mandibular deformity, webbed elbows and knees