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1,247 Possible Causes for Mild Dysmorphism

  • Cenani Syndactylism

    The present report suggests mild facial dysmorphism and quasidominant inheritance in one family with Cenani-Lenz syndrome.[ncbi.nlm.nih.gov] Mild facial dysmorphism (ptosis, high-arched palate, high, broad and prominent forehead, hypertelorism, flat nasal bridge, down slanting palpebral fissures, short nose, short[orpha.net] Both probands had similar mild facial dysmorphism; a high broad, prominent forehead, hypertelorism, a depressed nasal bridge, downslanting palpebral fissures, a short nose[ncbi.nlm.nih.gov]

  • Acidosis

    […] midline, synophrys, and a characteristic arched form of the eyebrows, along with mild hirsutism.[orpha.net] Clinical description Facial dysmorphism is characterized by a prominent forehead, wide nasal bridge, hypertelorism, broad anterior fontanelle, midfacial hypoplasia, broad[orpha.net]

  • Acanthosis Nigricans

    […] lumbar lordosis, or facial dysmorphism was observed, and only slight radiological abnormalities were noted.[jstage.jst.go.jp] In addition to the AN, he also exhibited a mild height deficit and macrocephaly, which prompted a search for FGFR3 mutations, although no skeletal disproportion, exaggerated[jstage.jst.go.jp]

  • Microdeletion 3q29 Syndrome

    Abstract The screening of individuals with mild dysmorphic features and mental retardation using whole genome scanning technologies has resulted in the delineation of several[ncbi.nlm.nih.gov] Martinez-Agosto Abstract The screening of individuals with mild dysmorphic features and mental retardation using whole genome scanning technologies has resulted in the delineation[empiregenomics.com] […] facial dysmorphism, developmental delay and variable congenital malformations.[ncbi.nlm.nih.gov]

  • Familial Adenomatous Polyposis

    dysmorphic signs and lower limb venous thrombosis.[ncbi.nlm.nih.gov] Raedle J et al. (2001) A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardation.[nature.com] 5q21.3-q23.3, encompassing the APC gene, associated with adenomatous polyposis and early colorectal cancer, hepatoblastoma, epidermoid cysts, mental retardation, several mild[ncbi.nlm.nih.gov]

  • Hypothyroidism

    […] syndromes (including Down’s syndrome) • Show mild TSH elevation of uncertain cause /- normal gland in situ Re-evaluation should be deferred until 2-3 years of age, depending[ncbi.nlm.nih.gov] […] do require re-evaluation can be broadly grouped into three categories; those who: • Were preterm and/or sick at the time of testing • Have congenital malformations and/or dysmorphic[ncbi.nlm.nih.gov]

  • Mixed Anxiety and Depressive Disorder

    […] most recent episode manic, With psychotic features 296.7F31.9Bipolar I disorder, Current or most recent episode unspecified 296.89F31.81Bipolar II disorder 300.7F45.22Body dysmorphic[dr-bob.org] 307.51F50.2Bulimia nervosa 305.90F15.929Caffeine intoxication 292.0F15.93Caffeine withdrawal 292.89Caffeine-induced anxiety disorder F15.180Caffeine-induced anxiety disorder, With mild[dr-bob.org]

  • Polyarthritis

    Systemic findings include mild craniofacial dysmorphism, dental and cardiovascular abnormalities, and redundant umbilical skin.[eyewiki.aao.org] […] craniofacial dysmorphism, dental abnormalities, and redundant umbilical skin.[eyewiki.aao.org] […] correctopia, ectropion uveae, and often is similar in clinical appearance to iridocorneal endothelial syndrome(ICE). [4] Systemically, patients with ARS will commonly have mild[eyewiki.aao.org]

  • Gastrointestinal Neoplasm

    […] leads to growth deficiency of prenatal onset (in 100% of patients), microcephaly (in 93%), mental retardation (in 72%), anomalies of the central nervous system (in 30%), mild[nejm.org] […] physical dysmorphic features, and cancer. 7 Worldwide, 37 cases of the mosaic variegated aneuploidy syndrome have been reported. 7-11 Biallelic mutations in the spindle-assembly[nejm.org]

  • Neonatal Adrenoleukodystrophy

    It is characterized by hypotonia, seizures, diffuse encephalopathy, sensorineural hearing loss, peripheral neuropathy, mild facial dysmorphism (hypertelorism and a flat midface[orpha.net] It is characterized by hypotonia, seizures , diffuse encephalopathy , sensorineural hearing loss , peripheral neuropathy , mild facial dysmorphism (hypertelorism and a flat[rarediseases.info.nih.gov]

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