Phenotype #0000299008

Individual ID 00406533
Associated disease RRS
Phenotype details short stature; prominent forehead; hypertelorism; no proptosis; long palpebral fissure; no epicanthus; no strabismus; no upslanted palpebral; downslanted palpebral; no ptosis; no long eyelashes; no midface retrusion; depressed nasal bridge; wide nasal bridge; short nose; abnormality of the nasal tip; anteverted nares; long philtrum; no short philtrum; no triangular mouth; downturned corners of mouth; thin upper lip vermilion; gingival overgrowth; bifid tongue; no micrognathia; no retrognathia; no high, narrow palate; no oral cleft; abnormality of the dentition; no melanocytic nevus; microtia; low-set ears; short neck; pectus excavatum; broad thumb; short palm; brachydactyly; no clinodactyly; no nail dysplasia; no syndactyly; no camptodactyly; no single transverse palmar crease; micropenis; no hypospadias; cryptorchidism; no sacral dimple; no abnormal heart morphology; no abnormality of the kidney; no hearing impairment; no inguinal hernia; scoliosis; rib fusion; mesomelia; hemivertebrae; no hip dislocation
Diagnosis/Initial Robinow syndrome
Inheritance Familial, autosomal recessive
Diagnosis/Definite RRS1
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-04-01 11:58:12 +02:00 (CEST)
Date last edited N/A

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