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Apert Syndrome

Apert syndrome and repercussions in Dental Medicine

Apert syndrome and repercussions in Dental Medicine

... The periosteum is a source of cells for bone remodelling, but its role in the development of craniosynostosis still needs further characterization. Yeh et al. [20] evaluated the proliferation, migration and osteogenic ...

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Apert syndrome: Factors involved in the cognitive development

Apert syndrome: Factors involved in the cognitive development

... - Apert syndrome is characterized by craniosynostosis, symmetric syndactyly and other systemic m a l f o rmations, with mental re t a rdation usually ...with Apert syndrome were studied, whose ...

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Braz. oral res.  vol.18 número1

Braz. oral res. vol.18 número1

... We have shown that Apert syndrome is a severe craniofacial dysostosis, with complex in- volvement of the face, calvaria and skull base. The combination and correlation of clinical evaluation and 3D-CT ...

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Caracterização do perfil de linguagem de indivíduos com Síndrome de Apert

Caracterização do perfil de linguagem de indivíduos com Síndrome de Apert

... The Apert Syndrome (AS) is considered a syndromic craniosynostosis that corresponds to 4,5% of all of the ...this syndrome can present abnormalities in the orofacial structures and hearing ...

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Rev. odonto ciênc.  vol.26 número1

Rev. odonto ciênc. vol.26 número1

... of Apert syndrome are well established and in agreement with the case described in the present ...The syndrome is clinically characterized by premature fusion of the coronal suture and hypoplastic ...

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Arq. NeuroPsiquiatr.  vol.65 número4A

Arq. NeuroPsiquiatr. vol.65 número4A

... with: Apert syndrome (a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial anoma- lies, and severe symmetrical syndactyly cutaneous and bony fusion of the hands and feet), ...

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POLYDACTYLY IN P FEIFFER SYNDROME II - OMIM #10160 0 A RARE  ASSOCIATION

POLYDACTYLY IN P FEIFFER SYNDROME II - OMIM #10160 0 A RARE ASSOCIATION

... craniosynostosis syndrome such as Antley-Bixler syndrome, Apert syndrome, Bearse-Stevenson syndrome, Crouzon syndrome, Muenke syndrome, and Pfeiffer ...Pfeiffer ...

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Pigment dispersion syndrome

Pigment dispersion syndrome

... iris insertion is typically posterior and the periph- eral iris tends to have a concave configuration. We report a case of pigment dispersion syndrome with posterior subcapsular cataract in both eyes in a young ...

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Síndrome Respiratória do Médio Oriente. Infeção pelo novo Coronavírus Middle East Respiratory Syndrome (MERS-CoV) – Normas de Orientação Clínica

Síndrome Respiratória do Médio Oriente. Infeção pelo novo Coronavírus Middle East Respiratory Syndrome (MERS-CoV) – Normas de Orientação Clínica

... Os doentes em investigação (casos prováveis) ou confirmados devem são internados de acordo com as indicações da Linha de Apoio ao Médico da DGS e, sempre que possível, em qu[r] ...

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High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups

High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups

... Ninety percent of patients with 22q11 deletion syndrome (22q11DS) have a dele- tion of approximately 3 million base pairs, while 7% have smaller deletions of 1.5 mil- lion bases (13). Similar to other syndromes ...

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Arq. NeuroPsiquiatr.  vol.70 número9

Arq. NeuroPsiquiatr. vol.70 número9

... limbs syndrome; however, in the patients with stif three-limbs or stif one-limb syndrome, it was not diagnostic, and the diag- nosis was conirmed after high serum anti-GAD antibodies had been ...

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Sleep overlap syndrome

Sleep overlap syndrome

... Pulmonary hypertension is observed in 75% of overlap patients and in only 12 –20% of undetected OSA patients (71). Overlap syndrome patients are 2.53 times more likely to experience tachyarrhythmias during sleep ...

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Sao Paulo Med. J.  vol.121 número3

Sao Paulo Med. J. vol.121 número3

... malignant syndrome was proposed, the patient was receiving re- peated neuroleptic ...malignant syndrome diagnosis and the relationship be- tween acute respiratory distress syndrome and neuroleptic ...

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PIRIFORMIS SYNDROME: A REVIEW

PIRIFORMIS SYNDROME: A REVIEW

... piriformis syndrome in many of ...piriformis syndrome is necessary for optimal ...piriformis syndrome, however, there is an obvious paucity of high-quality ...piriformis syndrome is also ...

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Peutz Jeghers syndrome

Peutz Jeghers syndrome

... Peutz-Jeghers syndrome (PJS) after previous surgical interventions for intestinal ...Peutz-Jeghers syndrome because of the risk of complications related to polyps, and the asso ciation with ...

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ABDOMINAL COCOON SYNDROME

ABDOMINAL COCOON SYNDROME

... CONCLUSION: Abdominal cocoon syndrome is a rare cause of small bowel obstruction. The non-specific clinical picture and imaging findings make it difficult to diagnose. In Indian settings it is most important to ...

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Medial Medullary Syndrome

Medial Medullary Syndrome

... Difüzyon beyin MRG’de bulbus sa¤ yar›s› medial tara- f›nda difüzyon k›s›tlamas› oluflturan akut iskemi ile uyumlu hipe- rintensite. Resim 4[r] ...

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HEAVY EYE SYNDROME

HEAVY EYE SYNDROME

... 2. Ruter T, Demer JL. Heavy eye syndrome in the absence of high myopia: a connective tissue degeneration in elderly strabismus patients. J AAPOS 2009. [Epub ahead of print] 3. Ejzenbaum F, Goldchmit M, Souza-Dias ...

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Syndrome in question

Syndrome in question

... MAGIC syndrome (mouth and genital ulcers with inflamed cartilage) is rare and groups together patients with this clinical picture without necessarily fulfill- ing the clinical criteria for Behçet's disease or ...

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Syndrome in Question

Syndrome in Question

... (Launois-Bensaude syndrome) affects both sexes equally, and is associated with a gynoid fat dep- osition pattern, with masses affecting the thighs and hips as well as the upper back and deltoid region, imparting a ...

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