Congenital renal cystic disease

Potter sequence is the atypical physical appearance of a baby due to oligohydramnios experienced when in the uterus. It includes clubbed feet, pulmonary hypoplasia and cranial anomalies related to the oligohydramnios. [Source: Wikipedia ]

May Cause

Renal cystic disease

May Be Caused by

 Common

Autosomal dominant polycystic kidney disease

Autosomal recessive polycystic kidney disease

Hepatic fibrosis-renal cystic disease

Potter sequence

Tuberous sclerosis

 Uncommon

Apert syndrome

Aplasia cutis congenita

Asphyxiating thoracic dysplasia

Asplenia syndrome

Axial osteomalacia

Bardet-Biedl syndrome

Beckwith-Wiedemann syndrome

Brachymesomelia-renal syndrome

Branchio-oto-renal syndrome

Caroli disease

Cerebro-costo-mandibular syndrome

Cutis laxa

Darier disease

DiGeorge syndrome

Ehlers-Danlos syndrome

Eronen syndrome

Femoral hypoplasia-unusual facies syndrome

Fetal alcohol syndrome

Fetal hydantoin syndrome

Fryns syndrome

Glomerulocystic kidney disease

Goldston syndrome

Hemihypertrophy

Joubert syndrome

Kaufman-McKusick syndrome

Lissencephaly

Marden-Walker syndrome

Meckel syndrome

Nail-patella syndrome

Nephronophthisis

Noonan syndrome

Oculo-auriculo-vertebral spectrum

Opitz trigonocephaly syndrome

Orofaciodigital syndrome type 1

Polysplenia syndrome

Renal-hepatic-pancreatic dysplasia

Roberts syndrome

Short rib-polydactyly syndrome type 1

Short rib-polydactyly syndrome type 2

Trisomy 13

Trisomy 18

Trisomy 21

Turner syndrome

Von Hippel-Lindau disease

Zellweger syndrome