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288 Possible Causes for Low Posterior Hairline, Turner Syndrome

  • Klippel-Feil Syndrome

    A 12-year-old female with Klippel-Feil syndrome (KFS) combined with Turner syndrome (TS) and a submucous cleft palate (CP) was presented.[] The clinical triad consists of short neck, low posterior hairline and limited neck movement. Multiple congenital anomalies have been associated with this disease.[] Klippel-Feil and Turner syndrome Klippel-Feil deformity, deafness and facial asymmetry Definition: A physical disorder that has material basis in abnormal segmentation of[]

  • Noonan Syndrome 1

    Mazzanti L, Cacciari E and the Italian study group for Turner syndrome (1998) Congenital heart disease in patients with Turner’s syndrome.[] posterior hairline Children [ edit ] Facial appearance lacks expression (resembles individual with myopathy) Adolescence [ edit ] Facial shape inverted triangle, wide forehead[] There is a relatively large head with a high forehead, low posterior hairline and a short uptilted nose.[]

  • Cornelia De Lange Syndrome

    Turner syndrome (TS) results from the partial or complete absence of one of the X chromosomes, usually associated with congenital lymphedema, short stature, and gonadal dysgenesis[] posterior hairline increased susceptibility to repeated respiratory infections Incidence [ edit ] congenital syndrome 1:10,000 to 1:100,000 (most accurate study showed 1:[] syndrome; and last, an interesting patient with a duplication of the SMC1A gene.[]

  • Blepharophimosis-Epicanthus Inversus-Ptosis Syndrome

    Congenital disorders such as Down syndrome , fetal alcohol syndrome , Cri du Chat syndrome , Klinefelter syndrome , Turner syndrome , Ehlers-Danlos syndrome , Waardenburg[] General examination revealed normal stature with absence of low set ears, short fourth metacarpal, shield chest, cubitus valgus, web neck and low posterior hairline.[] […] may be associated with trisomy 13, Turner syndrome, Cornelia de Lange syndrome, Noonan syndrome and Baraitser-Winter syndrome, among others. 4,5 Autosomal-dominant blepharophimosis-ptosis-epicanthus[]

  • Turner Syndrome

    A community for girls with Turner syndrome can help reinforce your self-esteem and provide you with a social network of people who understand your experience with Turner syndrome[] The patient showed the typical phenotype of Turner syndrome including distinctive dysmorphic features (short neck, low posterior hairline, wide position of nipples), aortic[] posterior hairline, nail dysplasia and lymphedematous hands and feet at birth Multiple genes involved in ovarian function, leading to gonadal dysgenesis and accelerated loss[]

  • Duchenne Muscular Dystrophy

    Turner syndrome is a relatively common chromosomal disorder which affects about one in 2000 live born females.[] No obvious phenotype of Turner syndrome was observed in this patient and cytogenetic analysis revealed that her karyotype is 46,X,i(X)(q10).[] The patient showed the typical phenotype of Turner syndrome including distinctive dysmorphic features (short neck, low posterior hairline, wide position of nipples), aortic[]

  • Rubinstein-Taybi Syndrome

    Trisomy 13 or Patau syndrome: The individual has an extra chromosome 13 Turner’s syndrome: Girls with Turner syndrome have one X chromosome and are missing all or part of[] […] 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[] , Christian Turner.[]

  • Ballard Syndrome

    The Turner's Syndrome Society web site has information on this study and others. top Links top References Lippe BM: Turner Syndrome.[] syndrome Cohen syndrome Gorlin-Goltz syndrome Turner syndrome 6 Cornelia de Lange syndrome 7 non syndromic hypertension : autosomal-dominant hypertension with brachydactyly[] Bonneman–Meinecke–Reich syndrome Bonnemann–Meinecke syndrome Bonnevie–Ullrich–Turner syndrome Book syndrome Boomerang dysplasia Booth– Haworth–Dilling syndrome Bor–Boy [[]

  • Premature Ovarian Failure

    Three girls diagnosed with Turner syndrome, 1 girl diagnosed with germ-cell tumor. and 1 girl diagnosed with lymphoblastic leukemia.[] She had epicanthal folds, long philtrum, high-arched palate, facial asymmetry, short webbed neck, low posterior hairline, mild scoliosis, cubitus valgus, mental retardation[] Karyotype revealed a mosaicism consistent with Turner syndrome.[]

  • Pterygium

    An 11.5-year-old girl with a working diagnosis of Turner syndrome (TS) was referred for her phenotypic features and growth retardation.[] It may be encountered in patients suffering from Turner syndrome or multiple pterygium syndrome.[] Pterygium of the neck, low posterior hairline, widely spaced nipples, cubitus valgus, upslanting palpebral fissures, hypertelorism, micrognathia, low-set ears, downturning[]

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