Inherited Renal Disorders Flashcards

1
Q

What is the most common inheritance of polycystic kidney disease

A

autosomal dominant

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2
Q

what is the most frequent life threatening hereditary kidney disease

A

Autosomal Dominant Polycystic Kidney Disease (ADPKD)

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3
Q

which chromosomes are the mutated genes found on in ADPKD

A
  • chromosome 16 (PKD gene1)
  • chromosome 4 (PKD2)
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4
Q

who develops end stage kidney failure earlier, patients with PKD1 mutation or PKD2 mutation?

A

PKD1 mutation

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5
Q

a) what size are normal kidneys
b) what size can they be in ADPKD

A

a) around 12cm
b) 20-25cm!

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6
Q

where do epithelial lined cysts arise from in ADPKD

A

a small population of renal tubules

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7
Q

ADPKD clinical features (renal)

A
  • reduced urine concentration ability
  • chronic pain
  • hypertension
  • haematuria
  • cyst infection
  • progression leads to renal failure
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8
Q

why may someone with ADPKD have haematuria

A
  • cyst rupture
  • cystitis
  • stones
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9
Q

what is the most common ADPKD extra renal manifestation

A

liver cysts

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10
Q

what percentage of ADPKD patients have intracranial aneurysms

A

4-8%

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11
Q

give 5 extra renal clinical features of ADPKD

A
  • liver cysts
  • intracranial aneurysms
  • cardiac disease (valve prolapse, valvular disease)
  • diverticular disease
  • hernias
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12
Q

what imaging is used to diagnose ADPKD

A

ultrasound

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13
Q

how many cysts are enough for diagnosis of ADPKD

A

2 or 3
(1 is enough in a high risk child)

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14
Q

what feature is seen more in autosomal recessive PKD as opposed to autosomal dominant

A

liver fibrosis

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15
Q

drug for ADPKD

A

tolvaptan

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16
Q

which chromosome is the faulty gene (PKDH1) found in ARPKD

A

chromosome 6

17
Q

in ARPKD, histologically, where are cysts seen appearing from?

A

the collecting duct system

18
Q

are kidneys palpable in ARPKD

A

yes

19
Q

Alports inheritance

A

x linked

20
Q

what is Alports syndrome a disorder of

A

type IV collagen matrix

21
Q

which gene is the mutation in in alports

A

COL4A5

22
Q

Alports syndrome manifestations

A
  • haematuria
  • proteinuria (seen later, confers bad prognosis)
  • sensorineural deafness
  • ocular defects (anterior lenticonus)
  • leiomyomatosis of oesophagus/genitalia - rare
23
Q

patient with microscopic haematuria +/- hearing loss, what should you suspect?

A

Alports syndrome

24
Q

Treatment of Alports

A

no specific treatment
- standard aggressive treatment of BP, proteinuria
- dialysis/transplantation eventually

25
Q

what is the deficiency in Anderson Fabry’s disease

A

a-galactosidase A

26
Q

what does Anderson Fabry’s disease affect

A
  • kidneys
  • liver
  • lungs
  • erythrocytes
27
Q

fabry’s disease clinical features renal

A
  • renal failure
28
Q

fabry’s disease cutaneous clinical feature

A

angiokeratomas

29
Q

fabry’s disease cardiac clinical features

A
  • cardiomyopathy
  • valvular disease
30
Q

fabry’s disease neuro clinical features

A
  • stroke
  • acroparaesthesia
31
Q

fabry’s disease treatment

A
  • enzyme replacement - fabryzyme
    and management of complications
32
Q

Medullary Cystic Kidney inheritance

A

autosomal dominant

33
Q

what’s the issue in Medullary Cystic Kidney

A

morphologically abnormal renal tubules leading to fibrosis

34
Q

where are cysts found in Medullary Cystic Kidney

A

corticomedullary junction / medulla

35
Q

diagnosis of Medullary Cystic Kidney

A
  • family history
  • CT scan
36
Q

where does Medullary Sponge Kidney get its name

A

in severe cases, medullary area appears like a sponge

37
Q

is renal failure common in medullary sponge kidney

A

no