Guest guest Posted April 30, 2011 Report Share Posted April 30, 2011 Hi Leehypophosphatesia 100%Differential ds with(copyed) Acatalasia Chediak-Higashi syndrome Chronic neutropenia Cyclic neutropenia Dentin dysplasia Hypophosphatasia Hypophosphatemic vitamin D resistant rickets Lesch-Nyhan syndrome Papillon-Lefèvre syndrome Sincerely LyudmylaFrom: Suvani Vasudevan <suvani.vasudevan@...>Subject: Re: NEW QUESTION Date: Friday, 29 April, 2011, 18:00 hello dr. avery,This is a condition of HYPOPHOPHATASIA, The Patients with this form typically present spontaneous shedding of primary teeth due to lack of cementogenesis. Almost always only the anterior primary uniradicular teeth( single rooted) are shed, multiradicular teeth as well as permanent teeth are not lost. There is no periodontal or gingival involvement, the pulp chamber of all teeth are larger than normal. This child has the infantile variety of hypophosphatasia. The incisors have been lost due to lack of periodontal attachment because of lack of cementum formation.hope it helps....vaniFrom: Dr Avery <avery_dr@...> Sent: Fri, 29 April, 2011 8:25:09Subject: NEW QUESTION Hi guysDespite the fact that today is a bank holiday(Royal Wedding) I want to challenge the group with this question.It came out in MJDF course...possibly will came smf similar in exams(MJDF,ORE)Boy 3 years,early loosing his teeth.Some teeth in the jaw are being loose...What condition it can be?Diff.Ds?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2011 Report Share Posted May 1, 2011 hi everyone, could someone plz help me with these questions: 1.What kind of discharge is seen in vesiculobullous lesions? 2.Which cells predominate in premonitary stage of RAS recurrent aphthous stomatitis?3.What is pethargy test? 4.Which oral lesion has autoantibodies to the intercellular substance of epithelial cells? 5.What is the name of the virus that do not clinically presents with ulcers on oral mucosa? From: Dr Avery <avery_dr@...> Sent: Fri, 29 April, 2011 8:25:09 AMSubject: NEW QUESTION Hi guysDespite the fact that today is a bank holiday(Royal Wedding) I want to challenge the group with this question.It came out in MJDF course...possibly will came smf similar in exams(MJDF,ORE)Boy 3 years,early loosing his teeth.Some teeth in the jaw are being loose...What condition it can be?Diff.Ds?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2011 Report Share Posted May 1, 2011 hi everyone, What is the extracranial cause of facial palsy1. cerebral malignancy 2.stroke 3.multiple sclerosis 4.Ransay hunt syndrome 5. Melkerson rosenthal syndrome thanks in advance siva. From: Lyudmyla Huhley <huhley2006@...> Sent: Sat, 30 April, 2011 9:32:31 AMSubject: Re: NEW QUESTION Hi Leehypophosphatesia 100%Differential ds with(copyed) Acatalasia Chediak-Higashi syndrome Chronic neutropenia Cyclic neutropenia Dentin dysplasia Hypophosphatasia Hypophosphatemic vitamin D resistant rickets Lesch-Nyhan syndrome Papillon-Lefèvre syndrome SincerelyLyudmyla From: Suvani Vasudevan <suvani.vasudevan@...>Subject: Re: NEW QUESTION Date: Friday, 29 April, 2011, 18:00 hello dr. avery, This is a condition of HYPOPHOPHATASIA, The Patients with this form typically present spontaneous shedding of primary teeth due to lack of cementogenesis. Almost always only the anterior primary uniradicular teeth( single rooted) are shed, multiradicular teeth as well as permanent teeth are not lost. There is no periodontal or gingival involvement, the pulp chamber of all teeth are larger than normal. This child has the infantile variety of hypophosphatasia. The incisors have been lost due to lack of periodontal attachment because of lack of cementum formation. hope it helps.... vani From: Dr Avery <avery_dr@...> Sent: Fri, 29 April, 2011 8:25:09Subject: NEW QUESTION Hi guysDespite the fact that today is a bank holiday(Royal Wedding) I want to challenge the group with this question.It came out in MJDF course...possibly will came smf similar in exams(MJDF,ORE)Boy 3 years,early loosing his teeth.Some teeth in the jaw are being loose...What condition it can be?Diff.Ds?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2011 Report Share Posted May 1, 2011 Ramsy hunt syndrome From: siva ranjani <siva2828@...> Sent: Sun, May 1, 2011 4:33:42 PMSubject: Re: NEW QUESTION hi everyone, What is the extracranial cause of facial palsy1. cerebral malignancy 2.stroke 3.multiple sclerosis 4.Ransay hunt syndrome 5. Melkerson rosenthal syndrome thanks in advance siva. From: Lyudmyla Huhley <huhley2006@...> Sent: Sat, 30 April, 2011 9:32:31 AMSubject: Re: NEW QUESTION Hi Leehypophosphatesia 100%Differential ds with(copyed) Acatalasia Chediak-Higashi syndrome Chronic neutropenia Cyclic neutropenia Dentin dysplasia Hypophosphatasia Hypophosphatemic vitamin D resistant rickets Lesch-Nyhan syndrome Papillon-Lefèvre syndrome SincerelyLyudmyla From: Suvani Vasudevan <suvani.vasudevan@...>Subject: Re: NEW QUESTION Date: Friday, 29 April, 2011, 18:00 hello dr. avery, This is a condition of HYPOPHOPHATASIA, The Patients with this form typically present spontaneous shedding of primary teeth due to lack of cementogenesis. Almost always only the anterior primary uniradicular teeth( single rooted) are shed, multiradicular teeth as well as permanent teeth are not lost. There is no periodontal or gingival involvement, the pulp chamber of all teeth are larger than normal. This child has the infantile variety of hypophosphatasia. The incisors have been lost due to lack of periodontal attachment because of lack of cementum formation. hope it helps.... vani From: Dr Avery <avery_dr@...> Sent: Fri, 29 April, 2011 8:25:09Subject: NEW QUESTION Hi guysDespite the fact that today is a bank holiday(Royal Wedding) I want to challenge the group with this question.It came out in MJDF course...possibly will came smf similar in exams(MJDF,ORE)Boy 3 years,early loosing his teeth.Some teeth in the jaw are being loose...What condition it can be?Diff.Ds?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2011 Report Share Posted May 2, 2011 Hi guysThe right answer isHYPOPHOSPHATASIA in some families is inherited as an autosomal dominant, affected individuals having a mild form of the syndrome. The majority of cases are inherited as an autosomal recessive. Hypophosphatasia is caused by a basic defect in the gene-encoding for tissue nonspecific alkaline phosphatase (TNSALP), the gene has been mapped to the short arm of chromosome 1 (1p36.1-34). TNSALP is also known as liver/bone/kidney alkaline phosphatase and in humans it hydrolyses phosphate from pyridoxal5'-phosphate, pyrophosphate and phosphoethanolamine. The resulting inorganic phosphate is utilized in the production of hydroxy-apatite crystals which are necessary for bone, enamel, dentin and cementum formation.Hypophosphatasia is characterized by diminished serum levels of alkaline phosphatase and the presence in the urine of phosphoethanolamine. The infantile variety is characterized by severe rickets, hypercalcemia and failure to thrive; this form is lethal. The juvenile variety is characterized by increased propensity to infections, bone deformities, costochondral junction enlargement called rachitic rosary, failure of calvarium to calcify and GI and renal problems. Patients with this form typically present spontaneous shedding of primary teeth due to lack of cementogenesis. Almost always only the anterior primary uniradicular teeth are shed, multiradicular teeth as well as permanent teeth are not lost. There is no periodontal or gingival involvement, the pulp chamber of all teeth are larger than normal.In the pic.. This child has the infantile variety of hypophosphatasia. The incisors have been lost due to lack of periodontal attachment because of lack of cementum formation. Teeth roots are not resorbed and there is horizontal atrophy of alveolar bone due to the fact that there is no cementum to provide periodontal ligament attachment and mechanical stimulation of the alveolus. The adult form is characterized by spontaneous fractures and bone changes similar to those seen in rickets but to a minor degree.Kind regardsLee From: Suvani Vasudevan <suvani.vasudevan@...>Subject: Re: NEW QUESTION Date: Friday, 29 April, 2011, 18:00 hello dr. avery, This is a condition of HYPOPHOPHATASIA, The Patients with this form typically present spontaneous shedding of primary teeth due to lack of cementogenesis. Almost always only the anterior primary uniradicular teeth( single rooted) are shed, multiradicular teeth as well as permanent teeth are not lost. There is no periodontal or gingival involvement, the pulp chamber of all teeth are larger than normal. This child has the infantile variety of hypophosphatasia. The incisors have been lost due to lack of periodontal attachment because of lack of cementum formation. hope it helps.... vani From: Dr Avery <avery_dr@...> Sent: Fri, 29 April, 2011 8:25:09Subject: NEW QUESTION Hi guysDespite the fact that today is a bank holiday(Royal Wedding) I want to challenge the group with this question.It came out in MJDF course...possibly will came smf similar in exams(MJDF,ORE)Boy 3 years,early loosing his teeth.Some teeth in the jaw are being loose...What condition it can be?Diff.Ds?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 5, 2011 Report Share Posted May 5, 2011 Hi guysWhat is the features of Gorlin-Goltz syndrom?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 5, 2011 Report Share Posted May 5, 2011 Hi KanikaThank you for a such comprehensive answerSincerely LyudmylaFrom: Kanika Kohli <kanika_sahil@...>Subject: Re: new question Date: Thursday, 5 May, 2011, 9:35 this is also known as jaw cyst basal cell nevus nd bifid rib syndrome.clinical features1.cuteneous anamolies,including basal cell carcinoma,other benign dermal cysts and tumors.2.dental and osseous anomalies,odontogenic keratocysts,mild mandibular prograthism,rib anamolies,vertebral anamolies3.ophthalmologic abnormalities,including hypertelorism with wide nasal bridge,congenital blindness4.neurologic anamalies,including mental retardation,dural calcification5.sexual abnormalities,including hypogonadism in males and ovarian tumors. biFrom: Dr Avery <avery_dr@...> Sent: Thu, 5 May, 2011 8:20:41 AMSubject: new question Hi guysWhat is the features of Gorlin-Goltz syndrom?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2011 Report Share Posted May 6, 2011 HI GUYS WITH WHAT NICKEL COATED IMPRESSION TRAYS SHOUL'D NOT BE DISINFECTED? THANK YOU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2011 Report Share Posted May 6, 2011 Sorry, just want to make sure. Are you asking the right or the wrong product to disinfect metal impression trays?From: ARTHUR TADEVOSYAN <arthur_tadevosyan@...> Sent: Fri, 6 May, 2011 14:11:28Subject: Re: NEW QUESTION HI GUYS WITH WHAT NICKEL COATED IMPRESSION TRAYS SHOUL'D NOT BE DISINFECTED? THANK YOU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2011 Report Share Posted May 6, 2011 Hello Lyumyla, Hello All, I am so happy that I passed part 2 . just recieved the results by email. thanks a lot Ludy for yr help and sipport and all the best to u and all the group members wants to clear ORE. Regards, Charlot/ Wameed From: Lyudmyla Huhley <huhley2006@...> Sent: Thu, May 5, 2011 1:31:03 PMSubject: Re: new question Hi KanikaThank you for a such comprehensive answerSincerelyLyudmyla From: Kanika Kohli <kanika_sahil@...>Subject: Re: new question Date: Thursday, 5 May, 2011, 9:35 this is also known as jaw cyst basal cell nevus nd bifid rib syndrome. clinical features 1.cuteneous anamolies,including basal cell carcinoma,other benign dermal cysts and tumors.2.dental and osseous anomalies,odontogenic keratocysts,mild mandibular prograthism,rib anamolies,vertebral anamolies 3.ophthalmologic abnormalities,including hypertelorism with wide nasal bridge,congenital blindness 4.neurologic anamalies,including mental retardation,dural calcification 5.sexual abnormalities,including hypogonadism in males and ovarian tumors. bi From: Dr Avery <avery_dr@...> Sent: Thu, 5 May, 2011 8:20:41 AMSubject: new question Hi guysWhat is the features of Gorlin-Goltz syndrom?Thank youLee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2011 Report Share Posted May 6, 2011 WRONG PRODUCT PLEASE MARCELA From: Marcela <marcesanchezf@...>Subject: Re: NEW QUESTION Date: Friday, 6 May, 2011, 15:10 Sorry, just want to make sure. Are you asking the right or the wrong product to disinfect metal impression trays? From: ARTHUR TADEVOSYAN <arthur_tadevosyan@...> Sent: Fri, 6 May, 2011 14:11:28Subject: Re: NEW QUESTION HI GUYS WITH WHAT NICKEL COATED IMPRESSION TRAYS SHOUL'D NOT BE DISINFECTED? THANK YOU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2011 Report Share Posted May 9, 2011 hello charlot ...congrats on passing part 2 . can u plz tell me wht material will i need for part 2 ...books n materials both..thanx in advance. > > > >From: Kanika Kohli <kanika_sahil@...> > >Subject: Re: new question > > > >Date: Thursday, 5 May, 2011, 9:35 > > > > > >Â > >this is also known as jaw cyst basal cell nevus nd bifid rib syndrome. > >clinical features > >1.cuteneous anamolies,including basal cell carcinoma,other benign dermal cysts > >and tumors.2.dental and osseous anomalies,odontogenic keratocysts,mild > >mandibular prograthism,rib anamolies,vertebral anamolies > >3.ophthalmologic abnormalities,including hypertelorism with wide nasal > >bridge,congenital blindness > >4.neurologic anamalies,including mental retardation,dural calcification > >5.sexual abnormalities,including hypogonadism in males and ovarian tumors.bi > > > > > > > ________________________________ > From: Dr Avery <avery_dr@...> > > > >Sent: Thu, 5 May, 2011 8:20:41 AM > >Subject: new question > > > >Â > >Hi guys > >What is the features of Gorlin-Goltz syndrom? > >Thank you > >Lee > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 22, 2011 Report Share Posted May 22, 2011 ....... this question has been repeated in the exam quite a few times. as far as i remember the question is... What is the percentage of oxygen in the blood which comes out of the lungs? > > What is the percentage of deoxygenated blood coming out of lungs? > > I think its 25 percent but not sure... > > Please reply > > Jas > Sent from my BlackBerry Torch® wireless device > Quote Link to comment Share on other sites More sharing options...
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