apabila keserabutan melanda *happy* :D

Assalamualaikum,,

Sekarang ni 2 pg, n aku masih kat depan laptop tenung tajuk2 assignment individual paediatric yg banyak,, kalau combine semua ada boleh mencecah 100+ condition yang kena include definition, sign and symptom, prognosis, clinical presentation, diagnosis, etiology, medical management n so on~~ due date 11/10

and assignment by group yg agak banyak jugak, and assignment medneuro intervention yg agak banyak jugak, and assignment medneuro assessement kena buat video~~ semua due date SAMA 11/10

and sekarang aku baru balik dari Shah Alam, ada hal..
plan ur time, insyaAllah... 
disebabkan semua pun update tajuk2 untuk semua condition, aku listkan je semua~~ senang sikit, 
serabut tengok kat fb,, =,="
tp thanks la kat semua, sebab semua dah list kan semua condition untuk setiap major area,, kalau tak jenuh nak cari condition apa,, sebab ada yg group, n yg individual kena buat SEMUA CONDITION YANG KAT BAWAH NI, NO PLAGIARISM! :p

U CAN DO IT MARYAM, INSYAALLAH :)

tajuk2 yg drpd group:

KENA ADA UNTUK SETIAP CONDITION

1) definition
2) sign and symptom
3) clinical presentation
4) pathophysiology/ etiology/ investigation
5) prognosis
6) medical management

CONGENITAL MALFORMATION
(GROUP 1-5)

group 1....(bone)

1.congenital limb deficiency
2. arthrogryposis multiplex congenita
3. osteogenesis imperfcta
4. sprengel's shoulder

5. congenital vertical-talus
6. congenital radio-ulna syntosis
7. congenital torticollis
8. congenital scoliosis
9. congenital dislocation/dysplasia of hip
10. congenital talipes equinovarus (clubfoot)
11. congenital deformities of skull
12. marfan syndrome
13. rational deformities (intoeing & outoeing)
14. blount's syndrome
15. achondroplasia (dwarf)
16. klippel-feil syndrome
17. leg length discrepancy

Aisyah Amirah Nurul Iffah Omar k.aida......

GROUP 2 (RESPIRATORY, CARDIAC)
RESPIRATORY MALFORMATION

PULMONARY SEQUESTRATION
CONGENITAL LOBAR EMPHYSEMA
CONGENITAL CYSTIC 
ADENOMATOID MALFORMATIONS
CYSTIC FIBROSIS
PULMONARY AGENESIS
PULMONARY HYPOPLASIA 

cardiac 
1. atrium septal defect
2. ventricular septal defect
3. tetralogy of fallot

4. patent ductus arteriosus
5. pulmonary stenosis
6. pulmonary atresia
7. aortic stenosis
8. bicuspid stenosis
9. bicuspid regurgitation

GROUP 3 (BRAIN)

Meningocoele/myelomeningocoele tu sejenis spina bifida. Jadi kena ubah sikit disorders which is:

1. anencephaly
2. microcephaly
3. macrocephaly
4. hydrocephalus
5. encephalocoele
6. spina bifida ( spina bifida occulta, meningcoele, myelomeningocoele, Myeloschisis & Craniorachischisis ) .

GROUP 4 (Chromosomal Abnormalities)

MAJOR
1. Kalmann's Syndrome
2. Adrenal Hypoplasia

3. Duchenne's & Becker's Muscular Dystrophies
4. Spinal Bulbar Muscular Atrophy
5. Severe Combined Immunodeficiency (SCID)
6. Lowe's Syndrome
7. Haemophilia B
8. Fragile X
9. Hunter's Syndrome
10. Angelman Syndrome

MINOR

1) agammaglobulinaemia
2) leschnyhan syndrome

3) adrenolenko dystrophy
4) haemophilia A
5) g6pp deficiency
6) ornithine transcarbamylase deficiency
7) wiskott-aldrich syndrome
8) testicular feminisation
9) anhydrotic ectodermal dysplasia
10) menkes kinky hair syndrome

GROUP 5 (GENETIC)

1) CHROMOSOMAL ABNORMALITIES :
* down syndrome (major)
* turner syndrome (major)

*klinefelter syndrome (major)

2) SINGLE GENE DISORDER :
*Autosomal Dominant Inheritance -hutington disease (major)
-ehiers danlos syndrome
*Autosomal Recessive Inheritance -thalassemia (major)
-sickle cell disease
*x-linked Recessive -colour blindness
*x-linked Dominant
*y-linked
*Mitochondrial or Cytoplasmic

3) MULTIFACTORIAL + POLYGENIC (COMPLEX) DISORDER :
* Spina Bifiida (major)
*cleft lip + palate

MOVEMENT DISORDERS

GROUP 6-9

GROUP 6 (INTRODUCTION OF MOVEMENT DISORDER)

1. maksud mov disorder tu gapo

2. prevalence khusunye kt malaysia

3. sign n symptoms secara umumnyer

4. cause pown secara general je

5. medical managemnt pown secara general

6. cari selain ataxic ,dyskinetic dll of mov disorder

GROUP 7: 

movement disorder (ataxia, dyskinesia, corticobasal degeneration)

1. ataxia ( Yantie Yan, Nabilah Hashim)
major types: 
a) cerebellar (dysfunction of cerebellum)
b) sensory (loss proprioception, sensitivity of joint)

C) vestibular (dysfunction of vestibular system)

minor: hereditary ataxia, autosomal dominant ataxias, autosomal recessive ataxias
*just briefly je

2. dyskinesia (MARYAM)
a) acute (off-period dystonia, diphasic dyskinesia, peak-dose dyskinesia)
b) chronic/ tardive (antipsychotic drug)
c) non motor (primary ciliary dyskinesia, biliary dyskinesia)

Hakim Zainal
3) corticobasal degeneration (rare- 6-8 years)
a) parkinsonism
b) alien hand syndrom
c) apraxia
d) aphasia

group 8

list of condition under MD
dystonia,herreditary spastic diplegia/tremor and myoclonus..

TREMOR

1. rest tremor
2.postural tremor
3.intention,action or kinetic tremor
4.mixed tremor
5.tremor caused by toxicities
6.tremor caused by psychiatric problems

MYOCLONUS
(pathophysiologic classification of myoclonus)
1. cortical
2. subcorticol
3. spinal

 Types of HEREDITARY SPASTIC DIPLEGIA:
1) pure - involved lower limbs only
2) complex - involved upper limbs and nervous system

group 9

tortolis : congenital muscular tortolis
acquired tortolis
tourette syndrome: motor/phonic tics
simple/ complex tics

-simple motor tics
-complex motor tics
-simple phonic tics
-complex phonic tics.
chorea 

DUE DATE: 11/10/2012

GO GO CYAIYOk MARYAM! :D

time: 2.37 a.m