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drfuntoosh
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05.16.08 (1 month ago)
#401
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| dev2020 wrote: |
| drfuntoosh wrote: |
regarding NHLstomach one option was surgery n chemotherapy remain mainstay of treatment
X ray skull in increased i.c.t. had ' sutural diastasis' as one of da options.........hope dis helps! |
drfuntoosh wrote:
dragonlives4ever wrote:
dev2020 wrote:
sorry dear,i haven't found the answer yet...will post once i find it
dear,
i dont think ans will change,u will be most welcome with new ans but proper explan and any ref net or book
btw whatz da answer as per u dragon??? hav u given it in earlier discussion????refering 2 hunter,hurler, gaucher q
YES I HAVE GIVEN ANS AS HUNTERS DS AT BOTTOM OF POST,BUT UNSURE ABT IT,NEED BETTER
BUT HUNTER'S IS A X-LINKED RECESSIVE DISEASE,SO MALES WILL BE EFFECTED. |
dats the biggest CRUX of it........but others are all AR.......if sum sex predisposition got 2 b there then disorder has 2 b sex linked , dat was the only logic I applied while going 4 HUNTER as ans...
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Adityapawar
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@dramitmittal
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05.16.08 (1 month ago)
#402
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i also marked met alkalosis option,but i doubt it coz logically also acdss is bettr
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dragonlives4ever
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05.16.08 (1 month ago)
#403
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| dev2020 wrote: |
| drfuntoosh wrote: |
regarding NHLstomach one option was surgery n chemotherapy remain mainstay of treatment
X ray skull in increased i.c.t. had ' sutural diastasis' as one of da options.........hope dis helps! |
drfuntoosh wrote:
dragonlives4ever wrote:
dev2020 wrote:
sorry dear,i haven't found the answer yet...will post once i find it
dear,
i dont think ans will change,u will be most welcome with new ans but proper explan and any ref net or book
btw whatz da answer as per u dragon??? hav u given it in earlier discussion????refering 2 hunter,hurler, gaucher q
YES I HAVE GIVEN ANS AS HUNTERS DS AT BOTTOM OF POST,BUT UNSURE ABT IT,NEED BETTER
BUT HUNTER'S IS A X-LINKED RECESSIVE DISEASE,SO MALES WILL BE EFFECTED. |
yaa ,u r right,i have not attempted the q uestion,but what do they mean by its mostly seen in females?
other diseases are autosomal.
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tulio
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05.16.08 (1 month ago)
#404
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Indan reference man a/e:
a) 60Kg
b) spends 8 hrs in bed
c) 20-39 years
d) consumes 2200Kcal/day
Ans: (d) consumes...
Ref: Park18th (Pg-457)
1)weighs 60 kg
2)spends 8hrs in bed, 4-6 hrs sitting & moving around and 2 hrs in walking & in active recreation or household duties
3)20-39 years
4)free from disease & physically fit for active work
on each working day, employed for 8 hrs that involves moderate activity
Read also Indian reference woman in next page.
Alas! none of us doctors are Indian reference men or women...reference- point no. 2 of my post!
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Adityapawar
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@reference male
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05.16.08 (1 month ago)
#405
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a reference male term is given to decide one who takes 1 unit which is quivalent to 2425 calories so 2200cal is not reference.
n i perfectly agree on other point with tulio that full fledged docs are not reference males(may be next nov AIIMS
they ask that  ) becoz:
1.they either consume too less or too much
2.sleep too less or too much
3 and most imprtntly papers like AIIMS
make them land into 40s or 45 before coming on field. 
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ReenaMittal
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05.16.08 (1 month ago)
#406
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ketoconazole
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dragonlives4ever
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05.16.08 (1 month ago)
#407
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| dragonlives4ever wrote: |
| life123 wrote: |
| dragonlives4ever wrote: |
which of the following diseases is transmitted by females?
a)hurlers disease
b)----------
c)---------
d)---------
can any one remember other options? |
ya dragon,,,other options were
a.hunter
b.hurler
c.schie
d.gaucher |
Traits or diagnoses known or suspected to be X-linked (at least in some forms of the diagnosis) are:
* Adrenoleukodystrophy
* Alport syndrome
* Androgen insensitivity syndrome
* Barth syndrome
* Becker's muscular dystrophy
* Centronuclear myopathy
* Charcot-Marie-Tooth disease
* Coffin-Lowry syndrome
* Color blindness
* Duchenne
* Fabry disease
* Fragile X syndrome
* Glucose-6-phosphate dehydrogenase deficiency
* Hemophilia A
* Hemophilia B (Christmas disease)
* Hunter's Syndrome
* Hypohidrotic ectodermal dysplasia
* Incontinentia pigmenti
* Kabuki syndrome
* Kennedy disease
* Lesch-Nyhan syndrome
* Menkes disease
* Myotubular myopathy
* Nonsyndromic deafness and X-linked nonsyndromic deafness
* Norrie disease
* Occipital horn syndrome
* Ornithine transcarbamylase deficiency
* Rett syndrome
* Simpson-Golabi-Behmel syndrome
* Spinal and bulbar muscular atrophy
* X-linked infantile spinal muscular atrophy (UBE1 gene)
* Wiskott-Aldrich syndrome
* X-linked agammaglobulinemia (XLA)
* X-linked ichthyosis
* X-linked Severe Combined Immunodeficiency (SCID)
* X-linked sideroblastic anemia
so answer may be hunters ds,what u all say? |
MPS II
Hunter disease (also referred to as mucopolysaccharidosis type II) is an X-linked recessive metabolic disease. In contrast to Fabry disease, women are very rarely affected. Hunter disease is one of a number of diseases called mucopolysaccharidoses (MPS), which are characterized by a defective degradation of mucopolysaccharides in the lysosomes. Hunter disease is caused by a defective gene, which is located on the X chromosome (Xq27.3-q28) and codes for iduronate-2-sulfatase.
Fabry disease
Previously, it was believed that symptoms almost exclusively occur in males due to the hereditary transmission. Since 2001, however, several systematically conducted studies (also here in Mainz) have shown that the condition is also found in females with great variability in clinical manifestations.
Danon disease
Danon disease
Danon disease is a subset of the lysosomal storage diseases with an X-linked inheritance and is characterised by a deficiency of the lysosomal protein LAMP-2. The predominant symptom in males is severe cardiomyopathy. Further signs and symptoms are general skeletal muscle weakness with a moderate increase in CK levels as well as mental retardation.
Danon disease should be considered as the cause of unexplained hypertrophic cardiomyopathy in young males. Females, who pass on the disease-causing gene, can also exhibit symptoms. Symptoms generally emerge later in females than males. The predominant clinical symptom is cardiac arrhythmias. Diagnosing the disease requires the creation of a family tree.
all are lysosomal storage dis ,out of which ,according to this extract ,hunter and fabry are found in female.
i may be wrong ,further discussion along with ref(net ,book,ebook,journal...any...) is welcome
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drfuntoosh
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05.16.08 (1 month ago)
#408
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@ aditya
very very witty one!!!!!!!!
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dev2020
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05.16.08 (1 month ago)
#409
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wrote:
drfuntoosh wrote:
regarding NHLstomach one option was surgery n chemotherapy remain mainstay of treatment
X ray skull in increased i.c.t. had ' sutural diastasis' as one of da options.........hope dis helps!
drfuntoosh wrote:
dragonlives4ever wrote:
dev2020 wrote:
sorry dear,i haven't found the answer yet...will post once i find it
dear,
i dont think ans will change,u will be most welcome with new ans but proper explan and any ref net or book
btw whatz da answer as per u dragon??? hav u given it in earlier discussion????refering 2 hunter,hurler, gaucher q
YES I HAVE GIVEN ANS AS HUNTERS DS AT BOTTOM OF POST,BUT UNSURE ABT IT,NEED BETTER
BUT HUNTER'S IS A X-LINKED RECESSIVE DISEASE,SO MALES WILL BE EFFECTED.
yaa ,u r right,i have not attempted the q uestion,but what do they mean by its mostly seen in females?
other diseases are autosomal
DAT'S WHAT IS MAKING IT CONFUSING.WONDER WHY THE AIIMS
PEOPLE GIVE SUCH A QUESTION...
IN ONE OF YHE QUESTIONS REGARDING STRUCTURES NOT SEEN BY BRONCHOSCOPY,THE QUESTION PAPER I HAD,ONE OF THE OPTIONS WAS SUBCRANIAL LYMPHNODES INSTEAD OF SUBCARINAL..
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dev2020
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05.16.08 (1 month ago)
#410
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condition which causes choroidal neovascularisation,all except
a.angiod streak
b.myopia
c.hypermetropia
ANS-HYPERMETROPIA
Neovascularization, Choroidal
Virtually any pathologic process that involves the RPE and damages the Bruch membrane can be complicated by CNV.
Degenerative conditions
ARMD
Myopia
Angioid streaks
Inflammatory or infectious conditions
Histoplasmosis
Sarcoidosis
Multifocal choroiditis
PIC
Choroidal tumors
Nevi
Melanoma
Hemangioma
Osteoma
Trauma
Choroidal rupture
Laser photocoagulation
Idiopathic
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