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Turner Syndrome
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Turner syndrome
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Genodermatoses
(9)
Female pseudo-Turner syndrome
Klinefelter syndrome
Apert syndrome
Zimmerman Laband syndrome
Acrocephal- osyndactylia
Acrocephal- osyndactylia
Treacher Collins syndrome
Leopard syndrome
Costello syndrome
Proteus syndrome
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Endocrinology
Growth hormone treatment
Idiopathic short stature
Kallmann syndrome
Adrenogenital syndrome
Syndromes
(32)
Parsonage Turner Syndrome
22q11.2 deletion syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Cri du chat syndrome
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Edwards syndrome
Williams syndrome
Russell-Silver syndrome
Trisomy 13
Xyy syndrome
Prader Willi syndrome
Warkany syndrome 2
Testicular feminization
Smith-Magenis syndrome
Wolf-Hirschhorn syndrome
Fragile x syndrome
Pierre robin syndrome
Syndrome
Female pseudo-Turner syndrome
Klinefelter syndrome
Apert syndrome
Zimmerman Laband syndrome
Treacher Collins syndrome
Leopard syndrome
Kallmann syndrome
Proteus syndrome
more...
Genetic disorders
(49)
Monosomy
Nail patella syndrome
Bardet Biedl Syndrome
Sakati-Nyh- an-Tisdale syndrome
Beckwith wiedemann syndrome
Beckwith wiedemann syndrome
Smith-lemli-opitz syndrome
48,xxxx
49, XXXXX
Trisomies
Chromosomal abnormalities
Chromosome 5q deletion syndrome
Partial trisomy
Laurence Moon syndrome
Friedreich ataxia
Branchio-Oto-Renal Syndrome
Timothy syndrome
Thrombocytopenia absent radius
Trisomy 22
Glutaricaciduria
Female pseudo-Turner syndrome
Klinefelter syndrome
22q11.2 deletion syndrome
Apert syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Cri du chat syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Treacher Collins syndrome
Donohue syndrome
Edwards syndrome
Williams syndrome
Trisomy 13
Xyy syndrome
Prader Willi syndrome
Warkany syndrome 2
Testicular feminization
Leopard syndrome
Smith-Magenis syndrome
Wolf-Hirschhorn syndrome
Fragile x syndrome
Kallmann syndrome
Costello syndrome
Adrenogenital syndrome
more...
Intersexuality
(28)
Gonadal dysgenesis
17-beta-hy- droxysteroid dehydrogenase deficiency
5-alpha-reductase deficiency
Adrenogenital syndrome
Androgen-induced hermaphroditism
Androgen-induced hermaphroditism
Breast binding
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
Genital reconstructive surgery
Hermaphrodite
Hermaphroditus
Imposex
Intersex Society of North America
Intersex conditions
Intersex people
Klinefelter syndrome
Lipoid congenital adrenal hyperplasia
Mixed gonadal dysgenesis
Organisation Intersex International
Progestin-induced virilisation
Pseudoherm- aphroditism
Sex assignment
Sex differentiation disorder
Swyer syndrome
Testicular feminization
Trans March
Transcending Boundaries Conference
True hermaphroditism
more...
Cytogenetics
(20)
Autosomal
Chromosome
Karyotype
Robertsonian
X chromosome
X chromosome
Chromosomal abnormalities
Chromosomal translocation
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Monosomy
Partial trisomy
Ploidy
Pseudoautosomal region
Synapsis
Tetrasomy
Trisomies
Uniparental disomy
more...
Congenital heart disease
Tricuspid atresia
Persistent truncus arteriosus
Sakati-Nyh- an-Tisdale syndrome
Congenital disorders
Cystic hygroma
Marinesco sjogren syndrome
Sunken chest
Keutel syndrome
Proteus syndrome
Diseases and disorders
Webbed neck
Cubitus valgus
Growth failure
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Yunis Varon syndrome
Trisomy 22
Symptoms
(8)
Short stature
Low set ears
Absent menstruation
Keratoconj- unctivitis sicca
Ptosis (eyelid)
Ptosis (eyelid)
Short height
Webbed neck
Growth failure
more...
Genetics
Chromosomes
Mosaicism
Nondisjunction
Xyy syndrome
Chromosome analysis
Medical condition
(54)
Male turner syndrome
Turner-like syndrome
Monosomy x
Acute myeloblastic leukemia with maturation
Growth hormone deficiency
Growth hormone deficiency
Tracheoesophageal fistula
Floating harbor syndrome
Triploidy
Ovarian dwarfism
Morvan disease
Acute megakaryoblastic leukemia
Female pseudo-Turner syndrome
Gonadal dysgenesis
Klinefelter syndrome
22q11.2 deletion syndrome
Nail patella syndrome
Bardet Biedl Syndrome
Apert syndrome
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Beckwith wiedemann syndrome
Ablepharon macrostomia syndrome
Cri du chat syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Fountain syndrome
Tricuspid atresia
Keutel syndrome
48,xxxx
Donohue syndrome
Edwards syndrome
Neonatal hyperbilirubinemia
Persistent truncus arteriosus
Chromosomal abnormalities
Trisomy 13
Xyy syndrome
Coarctation of the aorta
Partial trisomy
Prader Willi syndrome
Cystic hygroma
Friedreich ataxia
Testicular feminization
Fragile x syndrome
Branchio-Oto-Renal Syndrome
Marinesco sjogren syndrome
Sunken chest
Pierre robin syndrome
Timothy syndrome
Thrombocytopenia absent radius
Kallmann syndrome
Glutaricaciduria
Costello syndrome
Adrenogenital syndrome
Proteus syndrome
more...
Signs and tests
Estradiol
Serum follicle stimulating hormone levels
Serum luteinizing hormone levels
Karyotype
Complication
Arthritis
Cataract
Diabetes mellitus
Hashimoto's thyroiditis
Obesity
See also
(20)
Abl gene
FOXO1
Sex chromosome
Society of the United States
Epicanthal folds
Epicanthal folds
Gonadal
Neonatal hyperbilirubinemia
Hypertelorism
Coarctation of the aorta
Growth hormone
Bleeding tendency
PTPN11
Dermatoglyphics
Osteoporosis
Triple X syndrome
Www.turner- syndrome.org
MKL1
RBM15
Alpha-fetoprotein
Amenorrhea - primary
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