Main Article: Sex linkage X-linked recessive inheritance is a mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype...
15 KB (1,761 words) - 15:40, 28 March 2025
on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type. In medicine, X-linked dominant inheritance indicates...
8 KB (1,048 words) - 06:31, 2 June 2025
Sex linkage (redirect from X-linked inheritance)
gene. In humans, sex-linked patterns of inheritance are termed X-linked recessive, X-linked dominant and Y-linked. The inheritance and presentation of...
91 KB (9,955 words) - 21:47, 15 June 2025
characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. In X-linked recessive inheritance, a female with one...
13 KB (1,281 words) - 19:58, 2 May 2025
Genodermatosis (section X-linked recessive inheritance)
dermal hypoplasia and so on. The last kind is X-linked recessive inheritance, in this kind of inheritance, patients can be of any sex and the prevalence...
23 KB (2,533 words) - 11:38, 17 March 2025
X-linked ichthyosis (abbreviated XLI) is a skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in 2000...
20 KB (2,627 words) - 04:43, 26 May 2025
no longer diagnosed. The family history was consistent with X-linked recessive inheritance of intrauterine growth retardation and small head size, but...
2 KB (222 words) - 02:47, 28 October 2023
defective. It is an X-linked recessive inheritance trait, stemming from a mutated (abnormal) version of the IL2RG gene located on the X-chromosome. This...
36 KB (4,335 words) - 20:14, 12 July 2024
Hunter syndrome (category Commons category link from Wikidata)
tissues. Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. The symptoms of Hunter syndrome are comparable to those of...
22 KB (2,604 words) - 21:35, 16 June 2025
called alpha-thalassemia X-linked intellectual disability syndrome, nondeletion type or ATR-X syndrome, is an X-linked recessive condition associated with...
10 KB (1,059 words) - 01:01, 26 November 2024
Genetic disorder (redirect from X-linked syndrome)
disease. Some disorders are caused by a mutation on the X chromosome and have X-linked inheritance. Very few disorders are inherited on the Y chromosome...
35 KB (3,613 words) - 10:48, 25 March 2025
X-linked intellectual disability refers to medical disorders associated with X-linked recessive inheritance that result in intellectual disability. As...
19 KB (2,017 words) - 15:19, 25 May 2025
Blue diaper syndrome (category Autosomal recessive disorders)
characterized in 1964, and inherited in an autosomal recessive pattern although X-linked recessive inheritance has not been completely ruled out since reported...
7 KB (712 words) - 08:41, 2 January 2025
Haemophilia A (category X-linked recessive disorders)
almost exclusively in males born to carrier mothers due to X-linked recessive inheritance. Nevertheless, rare isolated cases do emerge from de novo (spontaneous)...
28 KB (2,934 words) - 01:29, 16 June 2025
automobile Megas XLR, an American animated television series X-linked recessive inheritance XL programming language runtime A321XLR, a variant of the Airbus...
863 bytes (147 words) - 19:21, 27 September 2024
Leukodystrophy (section X-linked adrenoleukodystrophy)
at 1 in 7,600. The majority of types involve the inheritance of an X-linked recessive, or X-linked dominant trait, while others, although involving a...
35 KB (3,848 words) - 17:34, 10 May 2025
Duchenne muscular dystrophy (category X-linked recessive disorders)
muscle fibers' cell membrane integrity. The disorder follows an X-linked recessive inheritance pattern, with approximately two-thirds of cases inherited from...
68 KB (6,827 words) - 20:40, 29 May 2025
Aarskog–Scott syndrome (redirect from Facio digito genital syndrome recessive form)
Aarskog–Scott syndrome (AAS) is a rare disease inherited as X-linked and characterized by short stature, facial abnormalities, skeletal and genital anomalies...
9 KB (872 words) - 17:05, 18 April 2025
Chromosome abnormality (section Inheritance)
fibrosis. X-linked inheritance: Mutated X chromosomes may be inherited in a dominant or recessive manner. Within X-linked recessive inheritance, males are...
43 KB (4,583 words) - 11:56, 25 May 2025
X-linked genes are found on the sex X chromosome. X-linked genes just like autosomal genes have both dominant and recessive types. Recessive X-linked...
30 KB (2,485 words) - 20:40, 8 January 2025
Ichthyosis (redirect from Autosomal recessive congenital ichthyosis)
appearance, underlying genetic cause and mode of inheritance (e.g., dominant, recessive, autosomal or X-linked). Ichthyosis comes from Greek ἰχθύς (ichthys) 'fish'...
15 KB (1,008 words) - 14:16, 27 April 2025
Dominance (genetics) (redirect from Autosomal recessive inheritance)
sex chromosomes (allosomes) are termed X-linked dominant, X-linked recessive or Y-linked; these have an inheritance and presentation pattern that depends...
27 KB (2,826 words) - 05:14, 12 June 2025
principle of dominant inheritance discovered by Mendel states that in a heterozygote the dominant allele will cause the recessive allele to be "masked":...
38 KB (4,045 words) - 18:23, 23 May 2025
group of familial disorders, including X-linked recessive nephrolithiasis with kidney failure, X-linked recessive hypophosphatemic rickets, and both Japanese...
12 KB (1,247 words) - 18:51, 24 May 2025
non-syndromic syndactyly/synostosis. Autosomal dominant and X-linked recessive inheritance patterns have been reported. The fusion of two or more metacarpal...
9 KB (867 words) - 00:17, 27 May 2025
Blue-cone monochromacy (redirect from Achromatopsia incomplete, X-linked)
(L) and green (M) cone photoreceptor cells in the retina. BCM is a recessive X-linked disease and almost exclusively affects XY karyotypes. Cone cells are...
19 KB (2,129 words) - 01:04, 28 March 2025
dislocations of multiple joints. It is believed that this disease's inheritance is X-linked recessive. The most characteristic signs and symptoms of SCARF syndrome...
15 KB (1,320 words) - 18:31, 25 May 2025
Non-Mendelian inheritance is any pattern in which traits do not segregate in accordance with Mendel's laws. These laws describe the inheritance of traits linked to...
23 KB (2,657 words) - 00:48, 24 April 2025
disorders usually follow either autosomal recessive, autosomal dominant, x-linked recessive, or mitochondrial inheritance patterns. Oculocerebrofacial syndrome...
8 KB (495 words) - 06:35, 15 April 2024
X-linked recessive hypoparathyroidism is a rare, congenital form of hypoparathyroidism. The signs and symptoms of X-linked recessive hypoparathyroidism...
3 KB (201 words) - 13:11, 6 April 2023