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751 Possible Causes for Hypertrichosis of Eyebrows, Joint Range of Motion Increased, Long Lashes

  • Rubinstein-Taybi Syndrome

    Surgery resulted in complete pain relief, increased knee range of motion and marked improvement in the patient's gait.[] lashes, beaked nose, and high narrow palate), micrognathia, hirsutism, and low anterior hairline.[] The common abnormalities include hypertrichosis and hirsuitism,heavy eyebrows, prominent beaked nose,hypoplastic maxilla, lowest ears and skeletal anomalies including broad[]

  • Cerebro-Facio-Thoracic Dysplasia

    ), a narrow forehead and a short nose; there are also hypertrichosis (espec- ially posteriorly) and mental retardation.[] The facial appearance in the de Lange syndrome is very similar to that found in cerebro-facio-thoracic dysplasia, for there is synophrys (joining of the eyebrows in midline[]

    Missing: Joint Range of Motion Increased
  • Coffin-Lowry Syndrome

    RSK2 is a growth factor-regulated serine-threonine protein kinase, acting in the Ras-Mitogen-Activated Protein Kinase (MAPK) signaling pathway. Mutations in the RSK2 gene (RPS6KA3) on chromosome Xp22.2, have been found to cause Coffin-Lowry syndrome (CLS), an X-linked disorder characterized by psychomotor[…][]

    Missing: Long Lashes
  • Lytic Bone Lesion

    […] hyperflexibility Joints move beyond expected range of motion 0005692 Macrocephaly Increased size of skull Large head Large head circumference [ more ] 0000256 Narrow mouth[] […] eyebrows and lashes, prominent supraorbital ridges, hyper- telorism, micrognathia, highly arched palate, hick tongue, and stenotic ear canals (Fig. 1).[] […] of the medial part of the eyebrows” is present, meaning excessive hair growth in the patients’ eyebrow region, most likely leading to a unibrow. [ 6 ] The fourth symptom,[]

  • Hallermann-Streiff Syndrome

    Characteristic changes in the bones of the skull and the long bones of the arms and legs can usually be seen on x ray.[] The hair is usually sparse, particularly that of the scalp, brows, and lashes. Often there is no hair around the front and sides of the head.[]

    Missing: Hypertrichosis of Eyebrows
  • Congenital Disorder of Glycosylation Type 2A
    Missing: Joint Range of Motion Increased
  • Coffin-Siris Syndrome
    Missing: Joint Range of Motion Increased
  • Hajdu Cheney Syndrome

    The full text of this article hosted at is unavailable due to technical difficulties. Brief Report Mutations in NOTCH2 in families with Hajdu‐Cheney syndrome † Mark E. Samuels Corresponding Author E-mail address: Centre de Recherche de l'Hôpital Ste‐Justine, 3175, Cote Ste‐Catherine,[…][]

    Missing: Joint Range of Motion Increased
  • Wiedemann-Steiner Syndrome

    Affected individuals had long lashes, wide-set eyes, arched brows, a long philtrum (the space between the nose and the upper lip), short nose, low-set ears and a high palate[] […] cubiti, facial dysmorphism (hypertelorism, long eyelashes, thick eyebrows, downslanted, vertically narrow, long palpebral fissures, wide nasal bridge, broad nasal tip, long[] Facial characteristics include long eyelashes, thick or arched eyebrows with a lateral flare, and downslanting and vertically narrow palpebral fissures.[]

    Missing: Joint Range of Motion Increased
  • Mirhosseini-Holmes-Walton Syndrome

    Patients tend to have thick hair and eyebrows, long lashes, a peculiar eye shape (down slanting palpebral fissures and almond-shaped eyesantimongoloid slant or arched eyelids[] […] of upper lip (rare); [Ears]; Prominent earlobes (in some patients); Bilateral sensorineural hearing loss (in some patients); [Eyes]; High arched eyebrows; Sparse eyebrows[] Face]; High forehead; Frontal bossing; Malar flattening; Micrognathia; Retrognathia; Prognathism (rare); Facial asymmetry, mild (rare); Deviation of maxilla, slight (rare); Hypertrichosis[]