Level 2 conditions Flashcards

1
Q

Birth Asphyxia

A

Fetal hypoxia + increased co2 –> metabolic acidosis

Treatment:

  1. Endotracheal intubation
  2. Adrenaline
  3. Glucose/fluids if needed
  4. Phenytoin or diazepam if seizing
    • 72 hours Therapeutic cooling - 33.5 degrees
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2
Q
Birthmarks
Salmon patch
port wine stain 
strawberry naevus / infantile haemangioma
Mongolian spots
pigmented naevua
sebaceous navus
A
  • Salmon patch = pink mark on face + fades over 2 yrs
  • port wine stain = purple lesion, associated with sturge-weber syndrome–> fits
  • strawberry naevus = soft, raised red capillary, regresses by school years
  • Mongolian spots = blue lesion over bum/legs
  • pigmented naevus = moles, eg cafe au lait >4 may indicate neurofibromatosis

sebaceous navus = raised warty naeus on scalp

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3
Q

Cephalohaematoma

A

Blood between skull and scalp
Doesnt cross suture line
Can cause jaundice

Ddx = caput succadenum - crosses sutures

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4
Q

Haemolytic disease

A

Rhesus + Abo incompatability
Check with direct Coombs

Management: Rhesus prophylaxis, anti D igG at 28 weeks

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5
Q

Prematurity

Complications

A

Baby born before 37 weeks
Most issues before 32 weeks

Complications

  • Resp Distress + recurrent apnoea
  • Patent DA
  • Anaemia
  • Nec Ent
  • Intraventricilar haemorrhage
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6
Q

Resp distress dyrnome

A

Surfactant deficiency
Preterm, Fhx, C-section,

CF: cyanosis, tachypneaic, accessory muscles, grunting

IVX: CXR, bilateral ground glass, decreased lung volume

Management: Betamethasone or DEX steroids IM if preterm is imminent
Delivery room resus
Administer Abx until pneumonia is excluded
02 therapy CPAP

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7
Q

Small baby IUGR

A

Symmetrical small head and body = intrinsic eg downs syndrome

asymmetrical big head small body = Extrinsic factors eg maternal malnutrition or placental insufficiency

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8
Q

Talpies

Treatment?

A

Subluxation of talonavicular joint

Management: USS detection

Treatment: Early orthopaedic referred
1. PONSETI - conservative manipulation, repeated plaster caste, achilles tenotomy, boots and bars

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9
Q

Chicken pox

A

Varicella Zoster
Itubation 11-21 days

Presentation: rash on head and trunk lasting 2 weeks
Cant go back to school till lesions crusted over

Tx: Acyclovir used in severe cases or those immunisuppresed + paracetemol to control fever

Complications = fluclox if get infectious

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10
Q

Conjunctivitis

Treat with?

A

Neonatal conjunctivitis usually starts 3rd day of life. If complicated

–> Treat with Neomycin

Can be gonoccocal or chlamydial

Childhood conjunctivitis = red eyes and dischargne
Viral, bacterial and allergic

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11
Q

Food allergy

A

igE antibodies
Most common = milk, eggs, peanuts

Presentation: Bloody diarrhoea, mucus + abdo pain
FTT, eczema, anaphylaxis

Ivx = igE, exclude coeliac

Management: IM adrenaline in anaphylaxis, most resolve by 2 years except peanut

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12
Q

Infectious mononucleosis

A

90% caused by EBV /CMV

Prodrome: 3-5 days, headache, low grade fever
Syx: exudative pharygitis, tender lumps, hepatosplenomegaly

Ivx: FBC, monospot test

Treatment: Supportive care for syx, avoid contact sport for 1 month

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13
Q

Kawasaki disease

1,2,3,4,5
1 = tongue strawberry
2 = eyes
3 = lymph nodes
4 = limbs (rash) palms and soles 
5 = days temp
A

Onset 6 months - 4 years
Self limiting vasculitis
Diagnosis = warm CREAM

5 day temp >38.5
Conjunctivitis bilateral
Rash
Erythema on palms and soles
Adenopathy
Mucus membranes involved = dry strawberry tongue 
RISK coronary artery aneurysms!!!!

IVX: bloods, ECG, echo

Treament: High dose, Immunoglobulins IVIg wihtin 10 days
+ Aspirin (only time allowed as can cause reyes syndrome = rapidly progressive encephalopathy)

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14
Q

Measles

A

Young children
Incubation 8-12 days

(5Cs)
- KOLPICK SPOTS - white spots
- Cough
- Conjunctivits 
- coryza 
\+ fever + rash starts on face + spreads

Treatment: Prevention with vaccine
Immunocompromised give Ribavarin

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15
Q

Perioribtal cellulitis

do CT scan to check its not gone into eye to check its not orbital

A

Infection of peri-orbital skin around eye
Agents: S.aureus, may occur secondary to paranasal/ dental abcess.

Features: Fever, unilateral erythema, tenderness + oedema of eyelid

IVX: if severe and eye movements limited then refer to optimal/ ent

Tx: Ceftriaxone if eye movement visible and if not metronidazole

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16
Q

Brain tumours

30% are?
mean age?

A

30% are medulloblastomas. Mean age is 9y.
2X as common in boys.
Most are Gliomas = astrocytoma’s or medulloblastomas which
have spinal mets at diagnosis

Commonly presents with raised ICP.
Mostly cerebellar signs. DANISH Acronym
•Dysdiachokinesia, Ataxia, Nystagmus, Intention Tremor, Scanning dysarthria, Heel-Shin test positive

Syx: Papilledema, altered LOC, headache, vomiting, behavioural change, bulging fontanelle, raised BP, low HR
May exhibit focal neurological signs depending on site of tumour.

Management

  • MRI with contrast. Persistent back pain in children should always warrant an MRI.
  • Never do an LP if suspected raised ICP. Can cause coning.

Treatment
Surgery, Radiotherapy and Chemotherapy

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17
Q

Haemophillia

a =8
b=9

A

Only MEN affected
X -linked autosomal recessive clotting disorder

Syx depend on severity of haemophillia e.g easy brusiing

IVX: increased APPT , clotting screen

Treatment: lifestyle = avoid contact sports forever
IV factor 8 or 9 as prophylaxis

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18
Q

Leukaemia - most common in children?

lymphoma- most common in adolesence?
most common in childhood?

A
Acute Lymphoblastc Leukaemia (ALL=
always little people)
Most common childhood malignancy 
CF: weeks/days quick onset, malaise, anorexia, bone pain,  headaches
IVX: FBC = thrombocytopenia 
CXR identifies mediastinal masses 
Tx- chemo for 3 years 

Lymphoma?
Adolesence = Hodgkins due to EBV risk = reed sternberg cells
Childhood = Non hodgkins due to Burkitts
Tx = chemo

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19
Q
Sickle cell
Cause of crisis?
1. aplastic?
2. occlusion
3. haemolytic 
4. sequestration = sickling within organ

Management?
maintainance fluids?

A

Autosomal recessive HbSS = anaemia, HbSB = trait

  • Present with sudden pain in crisis
    1. aplastic due to infection eg PAROVIRS
    2. occlusion - thrombotic PAINFUL
    3. rare- hb drops
    4. sequesttrion pooling of blood in organ - abdo pain

ivx: blood film shows sickles cells

Management:

  1. Analgesia,
  2. 02
  3. keep warm + 38 degrees
  4. broad spec abx if temp
    • 150% normal mainatainance fluids

HbSS prophylaxis oral Pen V, folate supplements, vaccine and bone marrow transplant could cure

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20
Q

Inhialed foreign body

A

IVX: CXR with lateral views will show hyperinflation of infected side and mediastinal shift
Bronchoscopy to visualise object

Management: A-E
Effective cough –> encourage to cough
Ineffective + conscious = 5 back blows + 5 thrusts
Ineffective + unconscious = open airway, 5 rescue breaths –> CPR 15:2 in child, 3:1 neonate

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21
Q

Middle ear infection = otitis media

Examinaiton

treatment

A

Very common under 8 years old
Recurrent episodes can cause Glue ear = secretaory otitis media
Presentation:
Infants = high gever, irritability, head rolling, ear rubbing
older children = ear ache, deafness + discharge

Examination: Mild inflammation of tympanic membrane and dialated vessels on handle of malleus
Absent light reflex –> buldging TM and evenrually perforation and discharge.

Treatment: Calpol + allow to burst
If child systemically unwell = antibiotics - oral amoxicillin + paraceteol
if TM performates, can use topical abx eg ciprofloxacin

Surgery : gromet insertion for 1 year

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22
Q

Appendicitis

Ivx:

Management

A

Presentation: Pain aggrevated by movement, mild fever, centra abdo pain localised to Mcburneys RIF
Guarding, irritable, change in bowel habit

Ivx: Urinalysis abnormal in 1/3, bloods raised WCC + cRP,
USS 90% accurate in diagnosing

Management: Nil by mouth, A-E, Antibiotics, antiemeteics, analgesia, surgical review, appendicetomy

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23
Q

Coaelic disease

A

Intolerance to Gliadin
RF: Introduction of cereals before 4 months inc risk

Presentation: 8-24 months when starting solids, FTT, abdo distension, irritability, buttock wasting, pale floating stools

Ivx: If Serum tissue Transglutamase iGA (TTG), then small bowel endoscopy ans jejunal biopsy
Shows crypt hyperplasia and villous atrophy

Management: diet of excluding gluten
Risk of GI lymphoma if gluten ingested

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24
Q

Feeding problems
Should weigh?
Kwashikor vs Marsamus

A

Should weight 2X (age+4) e.g 2 X (5yrs+4) = 18 kg
Kwashikor = normal energy but inadequate protein so swollen abdomen
Marsimus = inadequate energy and protein

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25
Q

Inguinal hernia
more common in?

how to investigate?

A

8 times more common in boys
Mainly indirect and caused by patent processes vaginalus
More common on R side due to later sescent
Symptoms are rare = intermittent swelling in groin, occurs when crying, may be visible on cough

IVX: Transilluminaiton to exclude hydrocele
Management: Surgical Herniotomy asap to avoid incarceration

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26
Q

Intussusception

Key signs?

A
  1. Target sign on USS + small bowel obst on AXR
  2. Red current jelly stool 3
  3. Bile stained vomit
  4. Drawing up of legs

Management:

  1. Resusscitation of IV fluids
  2. Abx + analgesia
  3. NG if vomiting
  4. Air enema (radiologically guided air inflation within 12 hrs) - if doesnt work, surgiclal resection of gangrene bowel
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27
Q

Jaundice

Pre hepatic
Hepatic
Post hepatic

A

Pre hepatic -> unconjugated e.g. haemolysis such as spherocytosis

Hepatic –> Hepatocyte damage eg. hepatitis
= mixed conj and unconj sp Dark urine, normal stools

Post hepatic = conjugated
Obstruction of biliary drainage e.g. biliary atresia, cholecystitis
Dark urine, pale stoos + yellow skin and eyes

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28
Q

Mesenteric adenitis

A

Inflammation of lymph nodes in abdominal mesentry
Mimics acute appendicits - result of recurrent VIRAL

Presentaiton: central diffuse abdo pain (+ URTI)
Fever, malaise, usually resolves within 48 yrs
Pain less severe than appendix

Ivx: Observation- syx should improve
Large mesentaeric nodes seen at laporoscopy and normal appendix so no action needed

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29
Q

Pyloric stenosis
RF

Syx

treatment?

name of surgery?

A

-Progressive hypertrophy of pyloric muscle –> gastric outlet obstruction
4 X more common in boys
RF: Fhx, first born
Presentation between 2 + 7 weeks of age
- Vomiting non billous that increases in freq and intensity = PROJECTILE
- Hunger after vomiting and dehydration + weight loss
Olive shaped mass - palpable in R hypo
Ivx: test feeed and see peristalsis in abdo, USS to confirm
Blood gas for metabolic acidosis

Management: IV fluid restricton, NBM, empty stomach with NG tube - DRIP AND SUCK 48 hrs to correct electrolyte imbalance
Treatment: surgery = Ramstedts Pyloromyotomy

30
Q

Torsion of testicle
most common age?

Presentation:

A

MUST BE EXCLUDED in any child with scrotal pain
Most common 12 years old
RF: undescened testies

Presentaiton: Sudden onset severe pain, N+V, absent cremesteric reflex

Management: Must be relieved in 6-12 hrs to preserve via surgical exploration
CONTRALATERAL testies fixed also to prevent

31
Q

Undescended testies

investiations?
Treatment- palpable vs non palpable

A

Cryptochordism - more common in premature babies
Spontaneous descent may occurs in 1st 6 months of life

Exam: carried out in warm room attempt to bring testies down by sweeing massage in inguinal canal

If palpable = Can be treated with an Orchiopexy via inguinal incision
Impalpable = Laparoscopy to determine management as risk of malignant degeneration if in abdo

32
Q

Disorders of sexual development

  • Klinefelters
  • kallmans
  • Androgen insensitivity syndrome
A

Klinefelters = 47XXY = feminisation of male - taller than avergae, lack of secondary sexual charactersiics, infertile, gynaecomastic, small testies

kallmans = lack of smell with delayed puberty in BOY

Androgen insensitivity syndrome aka testicular feminisaiton = 46 XY
- Female phenotype with primary amenorrhoea, undescended testies but breast develop due to testosterone –> oestrogen

33
Q

Ambiguous genitaelia

Most common is Congenital adrenal hyperplasia

CF male + female

Treatment

A

CAH autosomal recessive disorder
90% cases caused by 21-hydroxxylase enzyme deficiency
Causes salt loss, hyperplasia of adnreal gland = Acute adrenal crisis

Females: Genitaelia look male - clitoral hyperplasia
Males: Enlarged penis, scrotum pigmented, bilateral. non-palpable undescended testies

IVx: Check Na, K, Glucose, pelvic US
Management: Medical + surgical emergency
Avoid immediate declaration of sex
Counselling for parents
+ STEROIDS FOR LIFE = Glucocorticoid + mineralocorticoids

34
Q

Precocious puberty

ages?

A
Less than 8 in girls and 9 in boys 
Central PP (true) = Gonadotrophin dependent e.g. intracrainal tumours. Puberty occurs due to early activation of hypothalamic gonadal axis

Peripheral PP = Gonadotrophin independent - e.g ovarian/testicular tumours - excess Sex steroidds

CF: premature puberty

Ivx: family history of puberty + evidence of growth acceleration?m

35
Q

Hypothyroidism

  • Congenital
  • Acquired

IVx

Treatment

A

Congenital = lack at birth and causes learning difficulty
Detected at screening in Guthrie test which shows high TSH and low T4.

Acquired: F>M, hashitmotos, dry skin, cold intolerance
Thyroid imaging and TFT

Management: Levothyroxine 10-15mg / kg a day

36
Q

Obesity

Drug Tx if severe

A

under 12 BMI > 98th centile, over 12 years = BMI over 30
Presentation: Fat and short = hypothyroid/ cushing
Fat + tall = feeding too much

Tx: Increase exercise, monitor diet
Orlistat if severe obesity

37
Q

Breath holding attack

Age group

A

Common aged 6 months to 18 months
Child upset, stops breathing and turns pale/grey- transient LOC. rapid full recovery

DDx = Reflex Anoxic seizure
- Sudden pain, deathly grey, syncope, stiff, convulsions.
Child wakes up drowsy

Management: stay calm and lie on side

38
Q

Epilepsy

A
Tonic = increased tone
Clonic = contractions 

Treatment:

  1. Acute = rectal diazepam or Buccal midazolam
  2. Sodium Valproate (not when female teenager)
  3. Carbamazepine for focal
39
Q

Head injury

A
A-E
Immediate CT scan if
 LOC < 5mins, suspicion of nonaccedental 
> 3 episodes of vomting
amnesia > 5 mins and abnoral drowsiness 

Tx: secure C spine, decompress, control ICP

40
Q

Hydrocephalus

Management

A

Obstruction of CSF flow

CF: large head, buldging fontanelle, fixed downward gaze

Ivx: measure head circumference, cranial USS

Management: Venticular peritoneal shunt 1st line

41
Q

Migraine

Treatment

A

10% with aura
Presentation: pulsating pain, N+V, photophobia, headache on awakening

Treatment:

  1. Simple analgesia
  2. Triptan
  3. Domperidone = antiemetic
  4. Prophylaxis with B blocker + Pizotifen (antihistamine)
42
Q

Plagiocephaly

A

Flat head syndrome

43
Q

Tics

Tourettes tx?

A

Twitch like movement
1 in 10 children - presents at 6 years
Worse when inactive and dissapears when concentrating
Management: ignore the tic,

Tourettes - motor and vocal tics
Management: Clonidine and Risperidone

44
Q

HAemolytic uraemic syndrome -HUS

TRaid?

Treatment?

A
Triad
1. Acute renal failure
2. Haemolytic anaemia 
3. Thrombocytopenia 
Most common cause AKI in children 

CF: Ecoli common cause-
Fever, vomiting, weakness + Bloody diarrhoea, liver jaundice

Ivx: bloods, anaemia, thrombocytopenia, stool and urine culture

Management: report to local authority
1. dialysis and ECULIZUMAB

45
Q

Nephrotic syndrome
commonest cause in kids?

How to treat this?

A
  • Proteinuria + low albumin and oedema
    No.1 Cause in kids = minimal change disease
    CF: oedema, periorbital when waking up

Management: hospitlise!!!

  1. Fluid restriction and low salt diet
  2. PREDNISOLONE 6 weeks
  3. Diuretics
  4. Penicillin during relapses

“mininmal change disease= dont see much change at the start of disease”

46
Q

Impetigo

A

Golden honey comb crust
Due to staph aureus
Highly contagious + complicates eczema

ivx- skin swab for sensitivity

Management: EXCLUSION FROM SCHOOL
Avoid itching Topical Fluclox if bullous
Non bullous - fusidic acid topic

47
Q

Nappy rash and thrush

A

Flexures spared!!
- Most commonly irritant dermatitis
Can cause 2 bacterial or candidial

Thrush =. Bright red rash clearly demarcated
Satellite lesions beyond border
tx: NYASTATIN cream and oral if needed

Management: Barrier cream, frequent changing of nappy
Severe = leave off nappy for a few days and steroid cream

48
Q

Stevens Johnsons

Cf

Management

A

SEVERE erythema multiforme
Affects skin, genitals, eyes and mucous membranes

CF: prodrome of fever, cough, sore throat
Abrupt rash –> widespread blisters and arthralgia

Management: ICU or burns unit
Hydration and emolient ointment
Systemic corticostroids
Identify cause (eg penicillin)

49
Q

Developmental dysplasia of hip

A

Congential dislocation as acetabulum is shallow and doesnt cover hip
CF: hip instability, subluxation
F>M, must resolve by 9 weeks of birth
Found at baby checks Barlow - dislocate and otolani re-locates

6 weeks- 4 months hip USS
4 months + x-ray

Management: PAVLICK harness, if doesnt work surgery

50
Q

Irritable hip / reactive arthritis
= reiters
cant see, pee, climb a tree

A

Autoimmunue attack on hoiny after GI or GU infection
Cause: Chlamydia, Shigella, group A strep rheumatic fever

CF: 1-4 weeks after infection develop joint swelling

Ivx: raised ESR and CRP, XR normal

Management: NSAIDS naproxen
Steroids
rheumatic fever = penicillnin

51
Q

Juvenille idiopathic arthritis

A

Under 16 years old- unkknow cause of autoimmune arthritis
Oligoarticular > 6 joints, poly 6+ or systemic

Cause: Synovium is targeted organ for inflammation
CF: swelling, joint pain, morning stiffness

IVx: rheumatoid factor, ANA+, ESR, cRP, imaging

Management: steroid joint injections, NSAIDs, methotrexate

52
Q

Limping child

A

RED FLAG = nocturnal pain, redness, swelling, stiffness, weight loss

pGals + urgent referral if <3 years or red flags

53
Q

Rickets / vit d deficiency

A

Cause: low sun exposure, low dietary intake, CKD, medications eg antiepileptics

CF: bowing of legs, delayed tooth eruption, progressive knock knees, skull softening, delayed walking

Ivx: ALP, phosphate, vit D and ca, u+es

Management: oral high dose vit D and Ca, safe sun exposure, diet

54
Q

Autistic spectrum disorder

A
  1. impaired social interaction
  2. Global impairment of speech and language
  3. Imposition of routines with ritualistic behaviour

Ivx: Refer to autism team + multidisciplinary support

55
Q

Blindness

A

Visual acuity <3/60 in one eye of child <16

56
Q

Deafness

A

Conductive e,g otitis media
Sensorineural eg genetic inherited, preterm, antenatal infection

ivx: otoscope and refer

57
Q
Developmental delay
Sit with support
- singles words 
- walks well 
- 2 word sentences 
6 blocks, 9 blocks
A

red flags

  • Sit with support 6 months old
  • singles words 1 years
  • walks well 18 months
  • 2 word sentences 2 years

6 blocks 2 years
9 blocks 3 years

58
Q

Anxiety

A

Syx: hyperarousal, heightened sense of danger, irritable

Management: CBT, SSRI and self help

59
Q

ADHD

Treatment?

Drugs?
How often to monitor and why

A

Impulsivity, Inattention and Hyperactivity

Treatment: Behavioural and family counselling - positive reinforcement
Educational intervention - involve school
Drugs: METHYPHENIDATE = RITALIN
- monitor weight and height every 6 months
SE: decreased appetite, poor sleep, tics

60
Q

Necrotising Enterocolitis

A

Common in pre-term and first week, formula fed babies

Presentation: Abdo distension, poor temp control, bloody stool, shock

Ivx: AXR, CRP, stool culture

Treatment; breast milk, If high risk give antenatal corticosteroids + abx prophylaxis
–> Nill by mouth, laporotomy resection

61
Q

Henoch Schoelen purpura triad

A

Arthritis, colicky abdo pain + purpuric rash in boys

62
Q

Delayed puberty

  1. Constitutional
  2. Hypothalamaic Hypogonadism
  3. Hypogonadotrophic Hypogonadism
A

Absence of puberty develpment by 14 for females and 15 for males

  1. Constitutional = family history of delay
  2. Hypothalamaic Hypogonadism = low FSH and LH due to chronic ilness eg chrons, malnutrition
  3. HypERgonadotrophic Hypogonadism = e.g Klienfelters, turners = high FSH and LH

ivx: LH, FSH, serum testosterone and estradiol, TFT

Tx: Tesosterone for male to induce sexual development and oestradiol in females

63
Q

Phenyketonuria

CF:

A

Autosomal recessive - Phelyalanine cant be converted to tyrosine present 6- 12 month sold
CF: Fair hair, blue eyes and eczema + –> Seizures
Musty odour

Ivx: Guthrie test + urinalysis. HIGH KETONES in urine

Management: dietary change to low phenylalanien + high tyrosine and protein food
monitor blood plasma phenylalaine regularly

64
Q

Slapped cheek

dangerous for?

A

PArovirus
Erythema infectiosum
Dangerous aplastic crisis in Sickle cell

65
Q

patent ductus arteriosus sound like?

Treat?

A

Continuous ‘machinery’ murmur

Treat = indomethacin or ibupofen = anti prostaglandin

66
Q

Croup memory aid

A

“para” troup

Parainfluenze

67
Q

bronchiolits memory aid

A

RSV=B

68
Q

7 S of innocent murmer

A
Soft
Systolic
Short
S1+2 normal
Standing and sitting variation 
symtomless
Special tests normal
69
Q

Dowsn syndrome complicatons
- cardiac?
others?

A
Cardiac = 
endocardial cushion defect + VSD
- Subfertility
- ALL 
- Alzheimers
- HIRSHSPRUNGS
-  Repeated resp infections
70
Q

time frame difference for Henoch-Schonlein purpura, and Post infectious glomerulonephritis?

A

HSP vasculiis = days after due to igA nephritis

Post infectious = several weeks after infection

71
Q

The first-line antibiotics for necrotising enterocolitis.

A

clindamycin and cefotaxime

72
Q

age for perthes disease?

A

under 8 - (i went to perth when i was 8)