Liphatsa tsa lefutso / bofokoli ba tsoalo
Sengoli:
Joan Hall
Letsatsi La Creation:
25 Hlakubele 2021
Ntlafatsa Letsatsi:
24 November 2024
- Lintho tse sa tloaelehang bona Mathata a Tsoalo
- Achondroplasia bona Ho tsieleha
- Adrenoleukodystrophy bona Leukodystrophies
- Khaello ea Alpha-1 Antitrypsin
- Amniocentesis bona Teko ea bakhachane
- Anencephaly bona Liphoso tsa Neural Tube
- Tlokotsi ea Arnold-Chiari bona Tlhahiso ea Chiari
- Ataxia bona Friedreich Ataxia
- Ataxia Telangiectasia
- Mathata a Tsoalo
- Mathata a Coagulation ea Mali bona Haemophilia
- Mathata a Boko, Liphatsa tsa lefutso tsa tlhaho bona Mathata a liphatsa tsa lefutso
- Malformations a Boko
- Maloetse a Kanavan bona Leukodystrophies
- Mathata a Cephalic bona Malformations a Boko
- Ho ba le lefu la boko
- Lefu la Charcot-Marie-Tooth
- Tlhahiso ea Chiari
- Sampling ea Chorionic Villi bona Teko ea bakhachane
- Cleft Lip le Palate
- Lelapa le Hloekileng bona Cleft Lip le Palate
- Hloekisa Mokokotlo bona Mokokotlo Bifida
- Ho kopanya
- Botšo ba 'Mala
- Mathata a Pelo ea Congenital
- Lefu la polokelo ea koporo bona Lefu la Wilson
- Lintho tse sa tloaelehang tsa Craniofacial
- Craniosynostosis bona Lintho tse sa tloaelehang tsa Craniofacial
- Cystic Fibrosis
- Down Syndrome
- Duchenne Muscular Dystrophy bona Muscular Dystrophy
- Ho tsieleha
- Ehlers-Danlos Syndrome
- Nalane ea Lelapa
- FAS bona Mathata a "Fetal Alcohol Spectrum"
- Mathata a "Fetal Alcohol Spectrum"
- Lefu la Fetal Alcohol Syndrome bona Mathata a "Fetal Alcohol Spectrum"
- Fetal Ultrasound bona Teko ea bakhachane
- Fragile X Syndrome
- FRAXA bona Fragile X Syndrome
- Friedreich Ataxia
- Khaello ea G6PD
- Lefu la Gaucher
- Phekolo ea liphatsa tsa lefutso le Gene
- Mathata a liphatsa tsa lefutso
- Tlhabollo ea lefutso
- Mathata a Liphatsa tsa lefutso
- Teko ea liphatsa tsa lefutso
- Khaello ea Glucose-6-phosphate Dehydrogenase bona Khaello ea G6PD
- Mathata a Pelo bona Mathata a Pelo ea Congenital
- Maloetse a Pelo, Congenital bona Mathata a Pelo ea Congenital
- Ho korotla ha pelo bona Mathata a Pelo ea Congenital
- Hemochromatosis
- Hemoglobin SS Mafu bona Boloetse ba Sickle Cell
- Haemophilia
- Phetoho ea Hepatolenticular bona Lefu la Wilson
- Morero oa Genome ea Batho bona Phekolo ea liphatsa tsa lefutso le Gene
- Lefu la Huntington
- Hydrocephalus
- Hypermobility Syndrome bona Ehlers-Danlos Syndrome
- Maloetse a Ts'oarellang ka Iron bona Hemochromatosis
- Klinefelter Syndrome
- Leukodystrophies
- Lefu la Maple Syrup Mafu bona Mathata a liphatsa tsa lefutso
- Lefu la Marfan
- Meriana le Boimana bona Bokhachane le Meriana
- Mathata a metabolism
- Mucolipidoses bona Mathata a metabolism
- Muscular Dystrophy
- Myelomeningocele bona Mokokotlo Bifida
- Liphoso tsa Neural Tube
- Neurofibromatosis
- Tlhatlhobo e sa tsoa tsoaloa
- Lefu la Niemann-Pick bona Mathata a liphatsa tsa lefutso
- Bula Mokokotlo bona Mokokotlo Bifida
- Osteogenesis Imperfecta
- Teko ea Bo-ntate bona Teko ea liphatsa tsa lefutso
- Phenylketonuria
- PKU bona Phenylketonuria
- Plagiocephaly ea maemo bona Lintho tse sa tloaelehang tsa Craniofacial
- Prader-Willi Syndrome
- Bokhachane le Meriana
- Teko ea bakhachane
- Progeria bona Mathata a Liphatsa tsa lefutso
- Maloetse a sa tloaelehang
- Rett Syndrome
- Ho hlahloba, lesea le sa tsoa tsoaloa bona Tlhatlhobo e sa tsoa tsoaloa
- Sickle Cell Anemia bona Boloetse ba Sickle Cell
- Boloetse ba Sickle Cell
- SMA bona Mokokotlo oa mesifa ea mesifa
- Mokokotlo Bifida
- Mokokotlo oa mesifa ea mesifa
- Maloetse a Tay-Sachs
- Tourette Syndrome
- Letšolo la Treacher-Collins bona Lintho tse sa tloaelehang tsa Craniofacial
- Trisomy 21 bona Down Syndrome
- TSC bona Tuberous Sclerosis (lefu la mokokotlo)
- Tuberous Sclerosis (lefu la mokokotlo)
- Turner Syndrome
- Usher Syndrome
- VHL bona Lefu la Von Hippel-Lindau
- Lefu la Von Hippel-Lindau
- von Mafu a Recklinghausen bona Neurofibromatosis
- Lefu la Wilson
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