Dispatches: First-cousin marriages

[Lozzer]

Did anyone else catch this? It was quite depressing. I've come to the conclusion that if you interbreed with your cousins in full knowledge of the risks: you deserve every infliction from the pain and suffering you've imposed onto your own children.

[PsychoSerenity]

No I missed it, but I did see the advert, and it surprised me. I always assumed it would take quite a few generations (10ish) for negative genetic effects to show from first-cousin inbreeding - and two or three from siblings. But I have no idea where I got that assumption from. Does anyone know how much inbreeding it takes to cause problems? Or even how to quantify inbred-edness?

[Lozzer]

No I missed it, but I did see the advert, and it surprised me. I always assumed it would take quite a few generations (10ish) for negative genetic effects to show from first-cousin inbreeding - and two or three from siblings. But I have no idea where I got that assumption from. Does anyone know how much inbreeding it takes to cause problems? Or even how to quantify inbred-edness?

Because they're Pakistani there's sufficient genetic background to have such a prolific problem within the Islamic community. Of course, theyse obscurantist morons have difficulty understanding this.

[maiforpeace]

No I missed it, but I did see the advert, and it surprised me. I always assumed it would take quite a few generations (10ish) for negative genetic effects to show from first-cousin inbreeding - and two or three from siblings. But I have no idea where I got that assumption from. Does anyone know how much inbreeding it takes to cause problems? Or even how to quantify inbred-edness?

All it takes is one generation. The offspring of first-cousins can be perfectly healthy, but the likelihood of miscarriage and congenital problems are increased, and become greater the closer the relatives are.

[Feck]

No I missed it, but I did see the advert, and it surprised me. I always assumed it would take quite a few generations (10ish) for negative genetic effects to show from first-cousin inbreeding - and two or three from siblings. But I have no idea where I got that assumption from. Does anyone know how much inbreeding it takes to cause problems? Or even how to quantify inbred-edness?

If one of your Grandparents has a recessive gene there is a 1/8 chance that your cousin will have the same gene ....We all carry many bad genes but because we have another working copy we never know . If your parents were cousins and you too marry a cousin then it's highly likely your children will have problems .

and Lozzer the parents and families may "deserve" the problems in your opinion(evil fucking attitude BTW ) but the children are innocent .

[Lozzer]

and Lozzer the parents and families may "deserve" the problems in your opinion(evil fucking attitude BTW ) but the children are innocent .

I never said the children weren't innocent, merely that the parents deserve the suffering they've inflicted. And why is it "evil"? Many of these people are flippant anti-science morons.

[Feck]

It's simple make cousin marriages illegal .

no persuading people, no pussyfooting around other peoples culture, make it illegal Now . If you want to marry a cousin you are already an idiot, what chance do your children have ?

The good news is that if Muslims keep this up then soon none of them will have the brains left to connect a battery to a detonator .

Because Lozzer it is fucking nasty to say to a woman that may have been forced to a greater or lesser degree into a marriage by her family that she Derserves to have disabled children. Even flippant anti-science morons don't deserve that .

[PsychoSerenity]

No I missed it, but I did see the advert, and it surprised me. I always assumed it would take quite a few generations (10ish) for negative genetic effects to show from first-cousin inbreeding - and two or three from siblings. But I have no idea where I got that assumption from. Does anyone know how much inbreeding it takes to cause problems? Or even how to quantify inbred-edness?

If one of your Grandparents has a recessive gene there is a 1/8 chance that your cousin will have the same gene ....We all carry many bad genes but because we have another working copy we never know . If your parents were cousins and you too marry a cousin then it's highly likely your children will have problems .

OK thanks, good to know.


Not that I was planning anything obviously.

[RuleBritannia]

As far as I'm concerned, incest between consenting adults is a victimless crime. Inbreeding is a different issue and should be treated as such.

[Feck]

As far as I'm concerned, incest between consenting adults is a victimless crime. Inbreeding is a different issue and should be treated as such.

Fine fuck your sister then but unless one of you has been sterilised it is a horrible thing to do .

[RuleBritannia]

As far as I'm concerned, incest between consenting adults is a victimless crime. Inbreeding is a different issue and should be treated as such.

Fine fuck your sister then but unless one of you has been sterilised it is a horrible thing to do .

LOL, overreact much?

[Lozzer]

As far as I'm concerned, incest between consenting adults is a victimless crime. Inbreeding is a different issue and should be treated as such.

Fine fuck your sister then but unless one of you has been sterilised it is a horrible thing to do .

I hope no one has autism here...

[Feck]

1
17-beta-hydroxysteroid dehydrogenase deficiency
2
2-Hydroxyglutaric aciduria
3
3-Methylcrotonyl-CoA carboxylase deficiency
6
6-Pyruvoyltetrahydropterin synthase deficiency
A
Abdallat Davis Farrage syndrome
Abderhalden–Kaufmann–Lignac syndrome
Abetalipoproteinemia
Ablepharon macrostomia syndrome
Acatalasia
Aceruloplasminemia
Acheiropodia
Acrocallosal syndrome
Acrodermatitis enteropathica
Acute fatty liver of pregnancy
Adducted thumb syndrome
Adenine phosphoribosyltransferase deficiency
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aicardi-Goutieres syndrome
Aldolase A deficiency
Alkaptonuria
Alpha-mannosidosis
Aminolevulinic acid dehydratase deficiency porphyria
Antley-Bixler syndrome
Apparent mineralocorticoid excess syndrome
Argininemia
Argininosuccinic aciduria
Arterial tortuosity syndrome
Aspartylglucosaminuria
Atelosteogenesis, type II
Atransferrinemia
Autosomal recessive multiple epiphyseal dysplasia
B
BIDS syndrome
Bare lymphocyte syndrome
Batten disease
Behr syndrome
Berdon syndrome
Bernard–Soulier syndrome
Beta-ketothiolase deficiency
Beta-mannosidosis
Bietti's crystalline dystrophy
Biotinidase deficiency
Bloom syndrome
Blue diaper syndrome
C
CAMFAK syndrome
Canavan disease
Carbamoyl phosphate synthetase I deficiency
Carnitine palmitoyltransferase I deficiency
Carnitine palmitoyltransferase II deficiency
Carnitine transporter deficiency
Carnitine-acylcarnitine translocase deficiency
Carnosinemia
Carpenter syndrome
Cartilage–hair hypoplasia
Cenani Lenz syndactylism
Cerebrotendineous xanthomatosis
Chédiak–Higashi syndrome
Cholesteryl ester storage disease
Chondrodystrophy
Chorea acanthocytosis
Chronic progressive external ophthalmoplegia
Citrullinemia
Cockayne syndrome
Compound heterozygosity
Congenital hepatic fibrosis
Congenital ichthyosiform erythroderma
Congenital adrenal hyperplasia
C cont.
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Congenital insensitivity to pain with anhidrosis
Craniodiaphyseal dysplasia
Cystathioninuria
Cystic fibrosis
Cystinosis
Cystinuria
D
D-Glyceric acidemia
DOOR syndrome
Diastrophic dysplasia
Dihydropyrimidine dehydrogenase deficiency
Donohue syndrome
Dubin–Johnson syndrome
Dubowitz syndrome
E
EAST syndrome
EEM syndrome
Ellis–van Creveld syndrome
Essential fructosuria
Ethylmalonic encephalopathy
F
Familial Mediterranean fever
Familial dysautonomia
Familial isolated vitamin E deficiency
Fanconi anemia
Farber disease
Fibrochondrogenesis
Finnish heritage disease
Fountain syndrome
Fraser syndrome
Friedreich's ataxia
Fucosidosis
Fukuyama congenital muscular dystrophy
Fumarase deficiency
G
GAPO syndrome
GM1 gangliosidoses
GM2-gangliosidosis, AB variant
Galactokinase deficiency
Galactose epimerase deficiency
Galactose-1-phosphate uridylyltransferase galactosemia
Galactosialidosis
Galloway Mowat syndrome
Gangliosidosis
Gastroschisis
Gaucher's disease
Gerodermia osteodysplastica
Giant axonal neuropathy
Gillespie syndrome
Gitelman syndrome
Glanzmann's thrombasthenia
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glutaric aciduria type 1
Glutathione synthetase deficiency
Glycogen storage disease type I
Glycogen storage disease type III
Glycogen storage disease type II
Glycogen storage disease type V
Phosphofructokinase deficiency
GM2 gangliosidoses
Griscelli syndrome
Guanidinoacetate methyltransferase deficiency
Gunther disease
H
Harlequin-type ichthyosis
Hartnup disease
Hemophagocytic lymphohistiocytosis
Hereditary pyropoikilocytosis
Hermansky–Pudlak syndrome
Histidinemia
H cont.
Holocarboxylase synthetase deficiency
Homocystinuria
Hurler syndrome
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypertryptophanemia
Hypervalinemia
I
IBIDS syndrome
ICF syndrome
Iminoglycinuria
Impossible syndrome
Infantile Refsum disease
Infantile free sialic acid storage disease
Infantile neuroaxonal dystrophy
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
J
Jansky-Bielschowsky disease
Jervell and Lange-Nielsen syndrome
Johanson–Blizzard syndrome
Juvenile Primary Lateral Sclerosis
K
Kapur-Toriello syndrome
Kaufman oculocerebrofacial syndrome
Keutel syndrome
Kindler syndrome
Kostmann syndrome
Krabbe disease
L
Lafora disease
Lamellar ichthyosis
Laron syndrome
Laurence–Moon syndrome
Lecithin cholesterol acyltransferase deficiency
Lethal congenital contracture syndrome
Letterer–Siwe disease
Leukocyte adhesion deficiency
Lipoid congenital adrenal hyperplasia
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Lucey-Driscoll syndrome
Lysinuric protein intolerance
M
MORM syndrome
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Marden-Walker syndrome
Meckel syndrome
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Meleda disease
Metachromatic leukodystrophy
Methemoglobinemia
Methylmalonic acidemia
Mevalonate kinase deficiency
Micro syndrome
Microvillous inclusion disease
Mismatch repair cancer syndrome
Mitochondrial neurogastrointestinal encephalopathy syndrome
Mitochondrial trifunctional protein deficiency
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysaccharidosis
Mulibrey nanism
Multiple sulfatase deficiency
N
N-Acetylglutamate synthase deficiency
Nakajo syndrome
Nemaline myopathy
Nephronophthisis
Netherton syndrome
N
Neuronal ceroid lipofuscinosis
Nezelof syndrome
Niemann-Pick disease, SMPD1-associated
Niemann-Pick disease, type C
Niemann–Pick disease
Nijmegen breakage syndrome
O
Ochoa syndrome
Ochronosis
Oculocutaneous albinism
Oculocutaneous albinism type I
Oculodentodigital dysplasia
Oguchi disease
Omenn syndrome
Ornithine translocase deficiency
Orotic aciduria
Otospondylomegaepiphyseal dysplasia
P
Papillon–Lefèvre syndrome
Pendred syndrome
Persistent Mullerian duct syndrome
Phenylketonuria
Pipecolic acidemia
Primary ciliary dyskinesia
Prolidase deficiency
Propionic acidemia
Pseudo-Hurler polydystrophy
Pseudodominance
Pseudoxanthoma elasticum
Purine nucleoside phosphorylase deficiency
Pycnodysostosis
P cont.
Pyruvate carboxylase deficiency
R
Rabson–Mendenhall syndrome
Raine syndrome
Rapadilino syndrome
Refsum disease
Renal dysplasia-limb defects syndrome
Renal-hepatic-pancreatic dysplasia
Reproductive compensation
Restrictive dermopathy
Roberts Syndrome
Rothmund–Thomson syndrome
Rotor syndrome
Rudiger syndrome
S
Sabinas brittle hair syndrome
Saccharopinuria
Salla disease
Sandhoff disease
Sanfilippo syndrome
Sarcosinemia
Short-chain acyl-coenzyme A dehydrogenase deficiency
Shwachman–Bodian–Diamond syndrome
Sickle cell trait
Sickle-cell disease
Situs inversus
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Sugarman syndrome
Survival motor neuron spinal muscular atrophy
T
Tangier disease
Tay–Sachs disease
Tetrahydrobiopterin deficiency
Thalassemia
Trimethylaminuria
Triosephosphate isomerase deficiency
Triple-A syndrome
Type I tyrosinemia
Tyrosinemia
Tyrosinemia type II
Tyrosinemia type III
U
Unverricht–Lundborg disease
Urbach–Wiethe disease
Urocanic aciduria
Usher syndrome
V
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Vici syndrome
W
Weissenbacher-Zweymüller syndrome
Werner syndrome
Wilson's disease
Wolcott-Rallison syndrome
Wolman disease
Woodhouse–Sakati syndrome
X
Xeroderma pigmentosum
Y
Yunis-Varon syndrome
Z
ZAP70 deficiency
Zazam Sheriff Phillips syndrome
Zunich–Kaye syndrome


you want the pictures too ?

and that is just the small list that I could find in a hurry
Isn't it just easier to avoid inbreeding by avoiding incest ?

[Lozzer]

Bernard–Soulier syndrome

I like the name Bernard.

[PsychoSerenity]

...
and that is just the small list that I could find in a hurry
Isn't it just easier to avoid inbreeding by avoiding incest ?

What are abortions for?