Gamuts

Fryns syndrome

Fryns syndrome is an autosomal recessive multiple congenital anomaly syndrome that is usually lethal in the neonatal period. Fryns (1987) reviewed the syndrome. [Source: Wikipedia ]

OrphaNet reference
Fryns syndrome 
May Cause
Absent digit
Agenesis or hypoplasia of the corpus callosum
Camptodactyly
Congenital heart disease
Congenital renal cystic disease
Congenital renal or ureteral anomaly
Corneal abnormality
Diaphragmatic hernia
External ear malformation
Gastroschisis
Genital anomaly
Hydrocephalus
Hydrops fetalis
Micrognathia
Nail aplasia
Nail deformity
Nail dystrophy
Nail hypoplasia
Neuronal migration disorder
Renal cystic disease
Supernumerary rib
Thick ribs
OrphaNet reference
Fryns syndrome 
May Cause
Absent digit
Agenesis or hypoplasia of the corpus callosum
Camptodactyly
Congenital heart disease
Congenital renal cystic disease
Congenital renal or ureteral anomaly
Corneal abnormality
Diaphragmatic hernia
External ear malformation
Gastroschisis
Genital anomaly
Hydrocephalus
Hydrops fetalis
Micrognathia
Nail aplasia
Nail deformity
Nail dystrophy
Nail hypoplasia
Neuronal migration disorder
Renal cystic disease
Supernumerary rib
Thick ribs


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