by Remember The Girls | Dec 31, 2022
Back to Previous Aarskog Syndrome Aarskog syndrome is a rare genetic condition characterized by short stature and multiple facial, limb and genital abnormalities. Additionally, some types of cognitive disorders may occasionally be present. Up to now, the FGD1 gene on...
by Remember The Girls | Dec 31, 2022
Back to Previous Acrogigantism (X-Linked) X-linked acrogigantism is the occurrence of pituitary gigantism in an individual heterozygous or hemizygous for a germline or somatic duplication of GPR101. X-linked acrogigantism is characterized by acceleration of linear...
by Remember The Girls | Dec 31, 2022
Back to Previous Adrenal Hypoplasia Congenita (X-Linked) X-linked adrenal hypoplasia congenita is a disorder that is noticeable from birth (congenital) and affects the development of the adrenal glands, which are hormone-producing (endocrine) organs (glands) located...
by Remember The Girls | Dec 31, 2022
Back to Previous Adrenoleukodystrophy X-linked adrenoleukodystrophy (ALD) is a rare genetic disorder that affects the white matter of the nervous system and the adrenal cortex. White matter is made up of nerve fibers called axons that relay nerve impulses from one...
by Remember The Girls | Dec 31, 2022
Back to Previous Agammaglobulinemia (X-Linked) X-linked agammaglobulinema is a primary immunodeficiency characterized by very low levels of immunoglobulins (proteins made by the immune system to help fight infections). People affected by this condition generally begin...
