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133 Possible Causes for Chin Dimples

  • SHORT Syndrome

    dimple, micrognathia, clinodactyly, partial lipodystrophy, hearing loss, functional heart murmur, delayed bone age, delayed speech, normal intellect, glucose intolerance,[ncbi.nlm.nih.gov] […] intrauterine growth retardation (IUGR) slow weight gain frequent illness triangular facies anteverted ears telecanthus deep set eyes wide nasal bridge hypoplastic alae nasi chin[radiopaedia.org] Other characteristics common in SHORT syndrome are a triangular face, small chin with a dimple, a loss of fat under the skin ( lipodystrophy ), abnormal position of the ears[en.wikipedia.org]

  • Craniofacial Dysplasia-Osteopenia Syndrome

    chin Chin butt Chin dent Chin dimple Chin skin dimple Indentation of chin [ more ] 0010751 Hearing impairment Deafness Hearing defect [ more ] 0000365 Mandibular prognathia[rarediseases.info.nih.gov] Depressed nasal bridge Depressed bridge of nose Flat bridge of nose Flat nasal bridge Flat, nasal bridge Flattened nasal bridge Low nasal bridge Low nasal root [ more ] 0005280 Dimple[rarediseases.info.nih.gov]

  • EDICT Syndrome

    Clinical diagnosis requires microstomia, whistling-face appearance (pursed lips), H-shaped chin dimpling, nasolabial folds, and two or more contractures of hands and feet.[fsrgroup.org] FSS is described as a myopathic distal arthrogryposis; diagnosis requires the following: microstomia, whistling face appearance, H-shaped chin dimpling, nasolabial folds,[fsrgroup.org] FSS is considered a type of myopathic distal arthrogryposis; diagnosis requires the following: microstomia, whistling-face appearance, H-shaped chin dimpling, nasolabial folds[fsrgroup.org]

  • Arthrogryposis Multiplex Congenita

    dimple, small wide-based nose, high palate, and small tongue.[slideshare.net] […] fingers and toes are accompanied by kyphosis, scoliosis, and malformations of the facial skeleton with characteristic facial appearance: narrow mouth, wide cheeks, an H-shaped chin[slideshare.net]

  • Branchio-Oculo-Facial Syndrome

    Other anomalies, in addition to the familiar cardinal features of BOFS, included facial nerve weakness (n 6), chin dimple or cleft of the lower lip (n 4), upper labial pits[ncbi.nlm.nih.gov]

  • Freeman-Sheldon Syndrome

    FSS can be distinguished from SHS by the presence of pouting lips, prominent nasolabial folds, and the characteristic chin dimple.[symptoma.com] FSS is considered a type of myopathic distal arthrogryposis; diagnosis requires the following: microstomia, whistling-face appearance, H-shaped chin dimpling, nasolabial folds[ncbi.nlm.nih.gov] FSS is described as a myopathic distal arthrogryposis; diagnosis requires the following: microstomia, whistling face appearance, H-shaped chin dimpling, nasolabial folds,[ncbi.nlm.nih.gov]

  • Widow's Peak Syndrome

    Dimples Freckles PTC testing Polydactyly Bent little finger Nearsightedness Mid-digit hair 13 14 Frequency of Dominant Alleles Dominant alleles are not necessarily more common[slideplayer.com] Big eyes are dominant over small ones, prominent noses dominate button noses, dimples and cleft chins are more common than smooth faces, thick lips beat out thin ones and,[babble.com] […] appearance, and the other (the recessive allele) has no noticeable effect on appearance 12 13 Human Traits with simple dominance : Widows peak Handedness Free earlobes Cleft Chin[slideplayer.com]

  • Trisomy 8q

    Symptoms - Chromosome 8- trisomy 8q * Prominent forehead * Small jaw * Retrognathia * Flat back of skull * Mandibular prognathism * Chin dimple * Large ears * Abnormal pinnae[checkorphan.org]

  • Trisomy 20p

    dimple , anteverted nares , CNS malformations, heart defects , psychomotor retardation and reduced life expectancy .[mondofacto.com] […] association with cardiac , skeletal , ocular and facial abnormalities . 20q13 trisomy shows brachycephaly , hypertelorism , ear anomalies , cleft palate , micrognathia , chin[mondofacto.com]

  • Cleidocranial Dysplasia

    chin Chin butt Chin dent Chin dimple Chin skin dimple Indentation of chin [ more ] 0010751 Hearing impairment Deafness Hearing defect [ more ] 0000365 Mandibular prognathia[rarediseases.info.nih.gov] Depressed nasal bridge Depressed bridge of nose Flat bridge of nose Flat nasal bridge Flat, nasal bridge Flattened nasal bridge Low nasal bridge Low nasal root [ more ] 0005280 Dimple[rarediseases.info.nih.gov]

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