Rickets Flashcards

(50 cards)

1
Q

what is the requirement of vitamin D of full term and when to start?

A

400IU\10ug\at birth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

requirement of preterm , twins and low birth weight of vitmain D and when ?

A

400-800IU\at the age of 1 month

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is the normal serum calcium

A

9-11mg\dl

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

normal serum of phosphate

A

4.5-5.5 mg\dl

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is the structure of normal bone

A

matrix osteoid and minerals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what are the bone layers

A

zone of resting cartilage :1layer
zone of profilerating cartilage:6-8
zone of degenerating cartilage:deposition of Ca and ph
zone fo calcification: invasion by BV and osteoblasts with minerlaization

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

define rickets

A

Defective minerlaization of the growing bone so disease of childhood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

pathophysiology of rickets

A
  1. proliferation without ossification
  2. epiphysis : failure of ca and ph depostion in the cartilage cells leading fo excess cartilage that invade the metaphysis(broadening and fraying
  3. diaphysis : bone rarefaction and fracture
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

types of rickets 4

A
  1. vitamin D deficiency rickets with 2ry ++parathyroidism:
    a. –intake of vitD b.malabsorption(small, large, liver, panceras
    c. hepatic disease(activation d. renal osteodystrophy(activation
  2. primary PO4 deficiency no 2ry ++parathyroid:
    a. X-linked hypophosphatemic rickets a. Fanconi syndrom: PCT dysfunction(gluco, phosphato, amino, uria
  3. end organ resistance to vit D
  4. hypophosphatasis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

types of rickets according to nutrition : and compare

A

nutritional vitamin D deficiency rickets : more common , 6month -2years , response to vitD good
Non-nutritional vit D de ric: less common , any age , poor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

etiology of nutritional vit D D rickets

A

a. inadequate intake of vit D : prolonged exclusive breast milk
cow milk: non optimum ca\ph ratio
b. inadequate sun exposure:
Wrapping Winter Windows Dark skinned people

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the rachitogenic diet

A

deficient in vit D ,, deficient in Ca and PO4
non optimum ca:p ratio +++ content of phytate or oxalates

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the first sign to appear in rickets

A

craniotabes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is the first sign to appear in rickets

A

craniotabes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the CP of the head in the skeletal rickets 5

A
  1. crainotabes: ping-pong ball sensation on pressing over the occiput=thinning
  2. frontal bossing
  3. macrocephaly
    4, delayed closure of AF
  4. delayed dentition
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

CP of limbs in rickets4

A

1.broadening of the ends of long bones
2.marfan sign: transverse groove across medial malleolus
3. deformities of the UL: convexity of the forearm if crawling
4. deformities of the LL:
genu varum: bow legs
genu valgum: knock knees
genu recurvatum: overextension of the knees

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

CP of chest in rickets 4

A
  1. rosary beads: cartilage proliferation at the costochondral junctions
  2. pigeon chest: ++AP diameter of the chest : protrusion of the sternum+rib flaring
  3. harrison sulcus:horizontal groove along the costal insertion of the diaphragm
  4. longitudinal sulcus: vertical groove behind rosary beads
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

cp of spine in rickets 4
due to laxity of ligament

A

kyphosis:correctable:DD of pott disease
scoliosis
kyphoscoliosis
lumber lordosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

CP of pelvis in rickest

A

contracted plevis important in females

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

CP of muscles and ligaments in rickets 3
hypotonia due to hypophosphatemia leading to

A

Delayed Downward Distension
1. delayed motor milestones;sitting , crawling , standing, walking
2. downward displacement of liver and spleen(visceroptosis)
3. abdominal distension dueto: hypotonia, visceroptosis not enlargement, constipation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

why ca is usually normal in rickets

A

due to 2ry hyperparathyroidism

22
Q

neurological manifestion in rikcets 2

A
  1. anorexia, irritability , sweating
  2. hypocalcemic tetany
23
Q

causes of hypocalcemia in rickets

A

parathyriod gland exhaustion
bone depletion: prolonged untreated
vit D:IM massive dose ; due to rapid mobilization of ca from blood to bone

24
Q

massive dose of vit D lead to hypocalciema

A

rapid mobilization of ca from blood to bone

25
latent tetany:serum, signs
Ca=7-9mg asymptomatic, only elicited by provocation
26
signs of latent tetany
chvostek sign: tapping of the facial nerve=twitches fo facial muscles trousseau sign:constriction of the UL by sphygmomanometer:carpal spasm peroneal sign: tapping of the peroneal nerve: pedal spasm
27
manifest tetay :serum
Ca;less than 7gm carpopedal spasm laryngospasm convulsions
28
manifest tetay :serum
Ca;less than 7gm carpopedal spasm laryngospasm convulsions
29
DD of rickets
1. delayed closure of AF 2. delayed dentition:rickets, ostogenesis imperfecta, down syndrom, hypothyroidism intracranial causes of macrocephaly(in AF only) 3. delayed walking
30
causes of delayed walking :neuro, bone, traing
1. neurological(central,periphral: cerebral palsy mental retardation hydrocephalus neuromusclar disorders 2.bone:rickets, trauma, fractures 3. training : by exclusion
31
causes of chest infection in rickets
hyptonia:weak cough chest deformities
32
causes of chest infection in rickets
hyptonia:weak cough chest deformities
33
complications of rickets 7
1. respiratory; chest infection, atelectasis 2. neurological: tetany, convulsions, laryngospasm 3. short stature:disproportionate 4.bone fractures and deformities 5.iron deficiency anemia: breast milk 6. contracted pelvis:obstructed labor in female 7. complications of treatment:++vit D
34
what is the type of short stature in rickets
disproportional
35
investigations in rickets
1.laboratory: serum Ca: usually normal ex in bone depletion, parp exuation, high dose of vit D serum phosphorus:--decreased serum alkaline phosphatase:++ increases Earliest manifestation 2. imaging:radiological improvment after 2 wks of vit D therapy
36
what is the earliest laboratory manifestation in rickets
++ alkaline phosphtase
37
when the improvment start to appear after ttt with D
2 weeks
38
see table in 67 rickets
39
prevention of rickets
nutritional education : breast, weaning, diet rich in D, avoid rachitogenic diet vit D supplementation sun exposure
40
dose and duration of vit D oral
3000-5000IU\day 2-4 weeks
41
dose and duration of vit D oral
3000-5000IU\day 2-4 weeks
42
dose duration advantages and dis of parenteral vit D3
600.000IU shock therapy duration:single IM dose adv:rapid, need no compliance, diagnosis of non vitamin D deficiency rickets dis:tetany, ++D
43
ttt of complication:tetany, deformities
iv Ca gluconate 10% 1ml\kg slowly orthopedic care after complete bone healing
44
CP of hypervitaminosis of vit D
Git:anorexia, nausea, vomiting, constipation renal: polyuria, polydipsia, renal stones
45
ttt of vit D ++
stop fluid steroids
46
calssification of non nutritional vit D D rickets
renal malabsorpstion hepatic
47
renal rickets
a. glomerular:renal osteodystrophy: defective activation by 1 a chronic kideny disease b. tubular: x-linked hypophosphatemic rickets fanconi syndrom cystinosis: fanconi+ corneal cystine crystal lowe syndrome: oculo- cerebro- renal:glucoma and cataract-MR-fanconi
48
malabsorption in rickets
cystic fibrosis celiac disease cholestasis
49
hepatic rickets
chronic liver disease:defective 25 hydr
50
hepatic rickets
chronic liver disease:defective 25 hydr