anomali congenital
DESCRIPTION
hematologiTRANSCRIPT
Prof. Dr. dr. Syarifuddin Rauf, SpA(K)Prof. Dr. dr. Syarifuddin Rauf, SpA(K)
Jabatan : Ketua Bagian Ilmu Kesehatan Anak FK-UNHAS
Spesialisasi : Anak Konsultan Ginjal & Hipertensi
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KIDNEY :KIDNEY :1.1. AGENESISAGENESIS : BILATERAL RENAL AGENESIS
= Potter’s Syndrome
Oligohydramnion
Pulmonary hypoplasia
Low-set ears
2.2. RENAL HYPOPLASIA :RENAL HYPOPLASIA : The kidney is small
Normal nephron
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3.3. Horseshoe kidney Horseshoe kidney :
Fusion of the renal parenchyma
Joined at the lower pole
4.4. Polycystic kidney :Polycystic kidney :
a. Infantile Polycystic Kidney (IPCK)
b. Adults Polycystic Kidney (APCK)
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I P C KI P C K
Autosomal Recessive Polycystic Kidney
Enlargement of distal tubulus & colligents
ductus
Glomerulus & proximal tubulus normal
Liver enlargement
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URETERURETER
Duplication of ureter
Ureterocele
Ectopic ureter
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VESICO URETERAL REFLUXVESICO URETERAL REFLUX
Reflux of urine from the bladder into ureter
Damage the upper urinary tract by bacterial
Infection
Causes : Congenital anomalous development
of the ureterovesical junction
Bladder outlet obstruction
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BLADDER (VESICA URINARIA)BLADDER (VESICA URINARIA)
Agnesia
Bladder neck obstruction
Agnesia / atresia urethra
Congenital posterior urethral valves
URETHRAURETHRA
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