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611 Possible Causes for Congenital Abnormality, Low Hairline, Low Set Ears

  • Turner Syndrome

    Other characteristics, like widely spaced nipples or low-set ears, also may lead to a suspicion of Turner syndrome.[] ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q90-Q99 Chromosomal abnormalities, not elsewhere classified › Q96- Turner's[] These include short stature, swelling, a broad chest, a low hairline, low set ears and a webbed neck.[]

  • Pelviscapular Dysplasia

    Category Congenital malformation Brite Human diseases [BR: br08402 ] Congenital malformations Other congenital malformations H00873 Cousin syndrome Human diseases in ICD-11[] […] posteriorly rotated and malformed external ears, dysplasia of conchae, small chin, short neck with redundant skin folds, low hairline, and mild psychomotor retardation.[] ears Abnormality of the pinna Stenosis of the external auditory canal Short neck Strabismus Deeply set eye Blepharophimosis Hypoplastic scapulae Hypoplastic ilia Brachydactyly[]

  • Rubinstein-Taybi Syndrome

    […] cardiac abnormalities: reported in up to 33% of affected patients 2 patent ductus arteriosus atrial septal defects ventricular septal defect hirsutism Most cases are thought[] […] anterior hairline Low frontal hairline Low-set frontal hairline [ more ] 0000294 Low hanging columella 0009765 Low posterior hairline Low hairline at back of neck 0002162[] […] syn·drome ( rū'bĭn-stīn tā'bē ), mental retardation, broad thumb and great toe, antimongoloid slant to the eyes, thin and beaked nose, microcephaly, prominent forehead, low-set[]

  • Noonan Syndrome

    . - It is difficult to look high in the sky at noon, therefore everything is down in NOONan syndrome- Low set ears, Downslanting eyes, Low posterior hair line, Low levels[] Noonan syndrome is a common genetic disorder that causes multiple congenital abnormalities and a large number of potential health conditions.[] […] posterior hairline Low hairline at back of neck 0002162 Muscular hypotonia Low or weak muscle tone 0001252 Scoliosis Abnormal curving of the spine 0002650 Strabismus Cross-eyed[]

  • Noonan Syndrome 3

    Concepts Disease or Syndrome ( T047 ), Congenital Abnormality ( T019 ) MSH D009634 ICD10 Q87.1 SnomedCT 205684007, 88327006, 205794007, 205824006 English Noonan Syndrome,[] Many children with Noonan syndrome have a short neck, and both children and adults may have excess neck skin (also called webbing) and a low hairline at the back of the neck[] hairline at the nape of the neck High hairline at the front of the head Large head Triangular face shape Broad forehead Short neck, webbed neck Eyes [ edit ] Hypertelorism[]

  • Saethre-Chotzen Syndrome

    ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q80-Q89 Other congenital malformations › Q87- Other specified congenital malformation[] The features of the syndrome include: turriplagiocephaly with a cranial circumference of 52 cm, facial asymmetry, low hairline, proptosis, antimongoloid slanting of palpebral[] Clinical features of this syndrome include unilateral or bilateral coronal synostosis, ptosis, low-set ears, hearing loss, hypertelorism, maxillary hypoplasia, deviated nasal[]

  • Disproportionate Short Stature - Ptosis - Valvular Heart Lesions

    Code Classification Congenital malformations, deformations and chromosomal abnormalities ( Q00-Q99 ) Other congenital malformations ( Q80-Q89 ) Oth congenital malform syndromes[] […] nuchal hairlineLow set ears • Cubitus valgus • Hypertrophic cardiomyopathy Turner’s syndrome • Short stature • Webbed neck • Low nuchal hairlineLow set ears • Cubitus[] He had dysmorphic triangular facies, hypertelorism, deep set eyes, down slanting palpebral fissures, low set ears, mild prognathia, and deep philtrum, prominent lower lip[]

  • Fetal Hydantoin Syndrome

    ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q80-Q89 Other congenital malformations › Q86- Congenital malformation syndromes[] hairlines.[] The characteristics associated with fetal hydantoin syndrome include distinct facial features, such as low-set ears, widely-spaced eyes, short nose, short neck, and a fold[]

  • Smith Lemli Opitz Syndrome

    Abstract Patients with Smith-Lemli-Opitz syndrome (SLOS) are born with multiple congenital abnormalities.[] He was a white male with an eunuchoid appearance, central obesity, a full head of graying hair, low anterior/posterior hairlines, and a clockwise hair whorl at the vertex.[] set ears and complex conchal formation, high-arched palate and thick maxillary alveolar ridges, and micrognathia.[]

  • Hallermann-Streiff Syndrome

    It is characterized by bird-like facies, dental abnormalities, hypotrichosis, atrophy of skin, congenital cataracts, bilateral microphthalmia, and proportionate nanism.[] There may be a low hairline. Read stories from people with Saethre-Chotzen on The Mighty .[] We describe a 20-year-old female patient whose clinical findings mostly fall into this syndrome, except for the presence of slightly low-set ears.[]

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