Ehlers-Danlos syndrome
Internal carotid artery dissection in a patient with Ehlers-Danlos syndrome type IV: diagnosis and management
... Ehlers-Danlos syndrome (EDS) type IV, also known as vascular EDS, is an inherited connective tissue disorder with an estimated prevalence of 1/100,000 to ...
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Loss of Col3a1, the gene for Ehlers-Danlos syndrome type IV, results in neocortical dyslamination.
... It has recently been discovered that Collagen III, the encoded protein of the type IV Ehlers-Danlos Syndrome (EDS) gene, is one of the major constituents of the pial basement membrane (BM) and serves ...
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Síndrome de Ehlers-Danlos em paciente com dor crônica. Relato de caso.
... 18. Voermans NC, Knoop H, van Engelen BG. High frequency of neuropathic pain in Ehlers-Danlos syndrome: an association with axonal polyneuropathy and compression neuropathy? J Pain Symptom Manage. ...
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SÍNDROME DE EHLERS-DANLOS TIPO HIPERMOBILIDADE: ESTRATÉGIAS DE INCLUSÃO
... of Ehlers-Danlos syndrome in the health field, as well as in ...of Ehlers-Danlos ...of Ehlers-Danlos syndrome and possible related learning disorders; seek ...
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Cervicoplastia na flacidez cutânea por síndrome de Ehlers-Danlos: relato de caso.
... The Ehlers-Danlos syndrome is a rare disorder characterized by multiples anomalies in collagen synthesis, structure and secretion, resulting in innumerous clinical manifestations such as cutaneous, ...
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Functional digestive symptoms and quality of life in patients with Ehlers-Danlos syndromes: results of a national cohort study on 134 patients.
... Our study has several limitations. The first one is the absence of control group (except regarding GIQLI for which we used a historical control French population) which precludes definitive conclusions from this survey. ...
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J. Appl. Oral Sci. vol.22 número3
... ehlers-Danlos syndrome, Beckwith-Wiedemann syndrome, Simosa syndrome, X-linked cleft palate and orofaciodigital syndrome 2,3,8,21,27. Additionally, maternal cocaine use is reported to[r] ...
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Obiteljski hipoplastični jezični frenulum : prikaz slučaja i rasprava o dijagnozi
... One of the most interesting and not yet understood anatomical structures of the oral cavity is the frenum or frenulum. The lingual frenum (LF) is an important structure that anatomically relates to the tongue and ...
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Pseudoaneurisma da artéria poplítea em um paciente com Síndrome de Ehlers-Danlos Tipo VI.
... 9. Onnessen BH, Sternbergh WC 3rd, Mannava K, Money SR. Endovascular repair of na iliac artery aneurysm in a patient with Ehlers-Danlos syndrome type IV. J Vasc Surg. 2007;45(1):177-9. ...
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Síndrome de Ehlers-Danlos e gravidez: relato de caso.
... Ehlers-Danlos syndrome is a connective tissue disease that is rarely associated with pregnancy, but with potentially fatal complications during pregnancy and puerperium, such as vascular and ...
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Dissecção da artéria carótida interna em paciente com síndrome de Ehlers-Danlos tipo IV: diagnóstico e manejo.
... Ehlers-Danlos syndrome (EDS) type IV, also known as the vascular type of EDS, is an inherited connective tissue disorder with an estimated prevalence between 1/100,000 and ...
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Tratamento endovascular de aneurisma de tronco braquiocefálico em paciente com síndrome de Ehlers-Danlos tipo IV.
... Ehlers-Danlos syndrome is a genetic disease that results in abnormalities of collagen synthesis, causing extremely fragile connective ...trunk; Ehlers-Danlos ...
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Arq. NeuroPsiquiatr. vol.70 número9
... Neurological disorders associated with glutamic acid decarboxylase (GAD) antibodies are rare pleomorphic diseases of uncertain cause, of which stiff-person syndrome (SPS) is the best-known. Here, we described nine ...
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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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High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups
... Congenital heart defects are the most common of all human birth defects. Numerous studies have shown that a deletion within chromo- some 22q11 is associated with DiGeorge syndrome and certain forms of sporadic ...
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Rev. Bras. Reumatol. vol.51 número3 en v51n3a09
... impingement syndrome, however, is rarely suspected in daily medical ...impingement syndrome was established, adequate therapy started, and satisfactory response ...
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Arq. NeuroPsiquiatr. vol.74 número1 X anp X20150155
... he Sneddon syndrome is a rare clinical syndrome that associates strokes and livedo, etiologically related with the antiphospholipid antibody syndrome (Figure 1) 1,2,3,4,5.. his [r] ...
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Reconstructing glacier-based climates of LGM Europe and Russia – Part 3: Comparison with GCM and pollen-based climate reconstructions
... 1996) meant that no explicit reconstruction of LGM ice depth was made. Temperature thresholds controlling the onset of ablation and proportionality of precipitation falling as rainfall or snowfall will only have a very ...
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Rev. bras.oftalmol. vol.74 número6
... We reported a rare syndrome with ophthalmologic manifestations and surgical indication to improve the vision. The visual symptoms are considered minor signs for the diagnosis, although the juvenile cataract may be ...
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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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