نتایج جستجو برای: nasal hypoplasia

تعداد نتایج: 52585  

Journal: :jentashapir journal of health research 0
mozafar sarafraz associate professor of otolaryngology, head and neck surgery, hearing and speech research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran soheila nikakhlagh associate professor of otolaryngology, head and neck surgery, hearing and speech research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; associate professor of otolaryngology, head and neck surgery, hearing and speech research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel: +98-9161111395, fax: +98-6132921838 hasan abshirini associate professor of otolaryngology, head and neck surgery, hearing and speech research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran mohammad momengharib assistant professor of radiology, ahvaz jundishapur university of medical sciences, ahvaz, ir iran payam haghpanah hearing and speech research centre, ahvaz jundishapur university of medical sciences, ahvaz, ir iran mojtaba jahani hearing and speech research centre, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

conclusions among anatomic variations, septal deviation and concha bullosa are predisposing factors for chronic sinusitis and we recommend that patients with chronic sinusitis be treated by surgical procedures. background identifying predisposing factors for chronic sinusitis is very important. objectives anatomical variation of the lateral nasal wall has been investigated in several studies an...

Journal: :بینا 0
احمد میرشاهی a mirshahi تهران- میدان قزوین- بیمارستان فارابی- مرکز تحقیقات چشم دانشگاه علوم پزشکی تهران آرش میرمحمدصادقی a mir mohammad sadeghi شهرستان خوانسار تاریخ لادن اسپندار l espandar

purpose: to report a case of proteus syndrome with new ophthalmic findings not reported elsewhere. patient and findings: the patient is an 18-year-old girl with red lesions on hand and foot from birth and disproportionate growth of right upper and lower limbs from the first year of life. on examination, the patient has enlargement of the right upper and lower limb, macrodactyly, vascular malfor...

Journal: :Journal of medical genetics 2011
Ute Moog Kerstin Kutsche Fanny Kortüm Bettina Chilian Tatjana Bierhals Neophytos Apeshiotis Stefanie Balg Nicolas Chassaing Christine Coubes Soma Das Hartmut Engels Hilde Van Esch Ute Grasshoff Marisol Heise Bertrand Isidor Joanna Jarvis Udo Koehler Thomas Martin Barbara Oehl-Jaschkowitz Els Ortibus Daniela T Pilz Prab Prabhakar Gudrun Rappold Isabella Rau Günther Rettenberger Gregor Schlüter Richard H Scott Moonef Shoukier Eva Wohlleber Birgit Zirn William B Dobyns Gökhan Uyanik

BACKGROUND Heterozygous mutations in the CASK gene in Xp11.4 have been shown to be associated with a distinct brain malformation phenotype in females, including disproportionate pontine and cerebellar hypoplasia. METHODS The study characterised the CASK alteration in 20 new female patients by molecular karyotyping, fluorescence in situ hybridisation, sequencing, reverse transcriptase (RT) and...

Journal: :Journal of medical genetics 2000
V Cormier-Daire M L Chauvet S Lyonnet M L Briard A Munnich M Le Merrer

We report on the association of absent patellae, genital and renal anomalies, dysmorphic features, and mental retardation in seven children (six boys and one girl) belonging to five unrelated families. Flexion deformities of the knees and hips with club feet and absent patellae were consistently observed and scrotal hypoplasia and cryptorchidism were present in all boys (6/6). Dysmorphic featur...

2000
Valérie Cormier-Daire Marie-Liesse Chauvet Stanislas Lyonnet Marie-Louise Briard Arnold Munnich Martine Le Merrer

We report on the association of absent patellae, genital and renal anomalies, dysmorphic features, and mental retardation in seven children (six boys and one girl) belonging to five unrelated families. Flexion deformities of the knees and hips with club feet and absent patellae were consistently observed and scrotal hypoplasia and cryptorchidism were present in all boys (6/6). Dysmorphic featur...

2014
Dong-Han Lee Kap Sung Oh

Unilateral nostril hypoplasia is an extremely rare congenital malformation of unknown etiology, and only a few cases have been reported in literature. Owing to variability and complexity of the deformity, surgical correction of unilateral nostril hypoplasia represents one of the most significant reconstructive challenges to reconstructive plastic surgeons. We report a 7-year-old Vietnamese chil...

2012
Smriti Rohilla Atul Kaushik V.C. Vinod Renu Tanwar Munish Kumar

Achondroplasia (Online Mendelian Inheritance in Man [OMIM] 100800), is considered as a form of skeletal dysplasia dwarfism that manifests with stunted stature and disproportionate limb shortening. Achondroplasia is of special interest in the field of dentistry because of its characteristic craniofacial features which include relative macrocephaly, depressed nasal bridge and maxillary hypoplasia...

2015
Bharesh K. Chauhan Jacqueline M. Hoover Hannah Scanga Anagha Medsinge Georgianne L. Arnold Ken K. Nischal

Craniofrontonasal syndrome (CFNS) is a rare X-linked disorder that shows greater severity in females and is largely attributed to mutations in EFNB1. A 7-year-old boy presented with hypertelorism, broad nasal root, midfacial hypoplasia, mandibular prognathia, ptosis, and scaphocephaly was clinically diagnosed with CFNS. Three-dimensional computed tomographic scans confirmed the isolated sagitta...

2014
P Bhargava S Khan R Sharma S Bhargava

Cleidocranial dysplasia (CCD) is an autosomal dominant disease with a wide range of expression, characterized by clavicular hypoplasia, retarded cranial ossification, delayed bone and teeth development, supernumerary teeth, stomatognathic, craniofacial and skeletal abnormalities. This paper presents a case of CCD in a female with brachycephalic skull, depressed frontal bone and nasal bridge, hy...

2008
Ikuyo Ohguro Hiroshi Ohguro

This is the first case report of a bilateral superior segmental optic hypoplasia (SSOH) accompanied by a glaucomatous optic neuropathy (GON). A 47-year-old man incidentally diagnosed as having bilateral SSOH, simultaneously disclosed glaucomatous optic disc appearances, including enlargements of the cup of the optic nerve heads and a thinning of the infero-temporal neuroretinal rim with laminar...

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