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1,004 Possible Causes for High Forehead

  • Prieto Syndrome

    […] growth * Skin dimple in lower back * Clinodactyly * Partially dislocated knee * Subcortical cerebral atrophy * Abnormal walk * Low set ears * Abnormal dermatoglyphics * High[] forehead 0000348 Hypertelorism Wide-set eyes Widely spaced eyes [ more ] 0000316 Inguinal hernia 0000023 Intellectual disability Mental deficiency Mental retardation Mental[] forehead * Broad nose * Wide set eyes * Reduced muscle tone * Small jaw * Seizures * Coxa valga * Extra teeth * Speech defect * Underdeveloped ear lobe * Undescended testes[]

  • Glutaric Aciduria

    Physical abnormalities are sometimes present and can include a large head (macrocephaly), high forehead, flat nasal bridge, malformed ears and genital abnormalities.[] Initial signs and symptoms may include: In the neonatal with anomalies form : Facial dysmorphism - high forehead, depressed nasal bridge, low-set abnormally formed ears Rocker[]

  • Neonatal Adrenoleukodystrophy

    forehead and large anterior fontanel, glaucoma, and impaired hearing.[] Mutations in genes PEX1/2/3/4/6/12/14/26 are responsible for ZS, which has clinical features of severe hypotonia, neonatal seizures, craniofacial dysmorphism such as high[]

  • Greenberg Dysplasia

    forehead 0000348 Horizontal sacrum 0003440 Hypertelorism Wide-set eyes Widely spaced eyes [ more ] 0000316 Hypoplasia of the maxilla Decreased size of maxilla Decreased size[] […] metaphysis Flared wide portion of long bone 0003015 Hepatic calcification 0006559 Hepatomegaly Enlarged liver 0002240 Hepatosplenomegaly Enlarged liver and spleen 0001433 High[]

  • Myopathy

    Affected infants often have distinctive facial features including a high forehead, underdevelopment of the middle of the face (midface hypoplasia), weakness of facial muscles[] Some infants have a narrow, high-arched roof of the mouth (palate) and later on develop severe misalignment of the teeth (malocclusion).[]

  • Saethre-Chotzen Syndrome

    forehead (56 percent), ptosis (53 percent), and prominent auricular crura (56 percent).[] Other symptions include: Head/Face: abnormally shaped head a high forehead a low frontal hair line facial asymmetry palatal anomalies [4] Eyes/Nose/Ears: droopy eyes (ptosis[] Symptoms of Saethre-Chotzen syndrome include the following: Craniosynostosis, usually of the lambdoid or coronal sutures High forehead Low set hairline Droopy eyelids Widely[]

  • Pyknodysostosis

    forehead, and dental abnormalities. 0000684 Frontal bossing 0002007 High forehead 0000348 Malar flattening Zygomatic flattening 0000272 Midface retrusion Decreased size of[] forehead, high narrow palate and dental abnormalities.[] […] with absent or small nails, an abnormal collarbone (clavicle), distinctive facial features including a large head with a small face and chin, underdeveloped facial bones, a high[]

  • Refsum Disease

    Craniofacial abnormalities reported include: high forehead; hypoplastic supraorbital ridges; epicanthal folds; midface hypoplasia; and large anterior fontanelle.[] FIGURE 1 Facial dysmorphism (high forehead, large anterior fontanelle, hypoplastic supraorbital ridges, epicanthal folds, and deformed earlobes) in the patient with IRD.[]

  • Craniofrontonasal Dysplasia

    forehead, and hypertelorism.[] Craniofrontonasal dysplasia (CFND) was diagnosed in a male child who had bilateral coronal craniosynotosis, midline facial clefting with cleft lip and palate, a broad and high[] Autopsy of the aborted male foetus showed the following features: High arched palate, a sloping forehead, flattened nose and receding chin, multiple joint contractures, particularly[]

  • Microphthalmia Syndromic 6

    forehead ; High palate ; Hypospadias ; Hypothyroidism ; Inferior vermis hypoplasia ; Lambdoidal craniosynostosis ; Low-set ears ; Macrotia ; Malar flattening ; Microcephaly[] forehead 0000348 Macrotia Large ears 0000400 Malar flattening Zygomatic flattening 0000272 Midface retrusion Decreased size of midface Midface deficiency Underdevelopment[] […] myelination ; Facial asymmetry ; Failure to thrive ; Female hypogonadism ; Finger syndactyly ; Flexion contracture of thumb ; Global developmental delay ; Hearing impairment ; High[]

Further symptoms