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[CYTOGENETICS] Pedigree & Genetic Counseling, Study notes of Cytology

Summary table about the characteristics and disorders of Recessive and Dominant Traits

Typology: Study notes

2024/2025

Available from 07/16/2025

archivealley
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[CYTOGENETICS]
PEDIGREE & GENETIC COUNSELING
PEDIGREE SHOWS TRAIT & DISEASE INHERITANCE
AUTOSOMAL RECESSIVE
AUTOSOMAL DOMINANT
X-LINKED RECESSIVE
X-LINKED DOMINANT
Y-LINKED
MITOCHONDRIAL
CHARACTERISTICS
two allele
one copy
father TO son
males, female equal
influence phenotype
influence phenotype
father TO daughter
father TO ALL daughter
holandric inheritance
TO ALL son & daughter
heterozygous parents no condition, carry allele
no symptom, until later in life / after reproductive age
males more affected
neither parent has trait, one child inherits
unknown affected, child inherits
after puberty
DISORDERS
cystic fibrosis
freckles
hemophilia
structural genes
basta ung mga 3 letters,
super dami nila
heteroplasmy
tay-sachs
polydactylism
red-green color blindness
incontinentia pigmenti
(skin lesions)
electron transport
maple syrup urine
huntington’s disease
x-linked ichthyosis
x-linked rickets
(bones soften/deform)
oxidative phosphorylation
process (neuro/myopathies)
phenylketonuria

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[CYTOGENETICS]

PEDIGREE & GENETIC COUNSELING

PEDIGREE SHOWS TRAIT & DISEASE INHERITANCE

AUTOSOMAL RECESSIVE AUTOSOMAL DOMINANT X-LINKED RECESSIVE X-LINKED DOMINANT Y-LINKED MITOCHONDRIAL

CHARACTERISTICS

two allele one copy father NO TO son father TO son males, female equal influence phenotype influence phenotype father TO daughter father TO ALL daughter holandric inheritance TO ALL son & daughter heterozygous parents no condition, carry allele no symptom, until later in life / after reproductive age males more affected neither parent has trait, one child inherits unknown affected, child inherits after puberty after puberty DISORDERS cystic fibrosis freckles hemophilia structural genes basta ung mga 3 letters, super dami nila heteroplasmy tay-sachs polydactylism red-green color blindness incontinentia pigmenti (skin lesions) electron transport maple syrup urine huntington’s disease x-linked ichthyosis x-linked rickets (bones soften/deform) oxidative phosphorylation process (neuro/myopathies) phenylketonuria