X-linked adrenal hypoplasia congenita
अंतिम अद्यतन 26 जुलाई 2023
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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 on top of each kidney. These glands produce a variety of hormones that regulate many essential functions in the body, such as response to stress.
विवरण
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 on top of each kidney. These glands produce a variety of hormones that regulate many essential functions in the body, such as response to stress.
One of the main signs of this disorder is adrenal insufficiency, which occurs when the adrenal glands do not produce enough hormones. Adrenal insufficiency typically begins in infancy or childhood and can cause vomiting, difficulty with feeding, dehydration, extremely low blood glucose (hypoglycemia), and shock. If untreated, these complications are often life-threatening.
Individuals with X-linked adrenal hypoplasia congenita may also have a shortage of male sex hormones, which leads to underdeveloped reproductive tissues, undescended testicles (cryptorchidism), delayed puberty, and an inability to father children (infertility). Together, these characteristics are known as hypogonadotropic hypogonadism.
The onset and severity of these signs and symptoms can vary, even among affected members of the same family.
Inheritance patterns
The source lists the following possible inheritance patterns: X-linked recessive. More than one pattern can apply in different cases.
Related genes
Other names
Adrenal hypoplasia congenita
X-linked AHC
Related patient information and medicines
Patient information leaflet
जन्मजात अधिवृक्क अतिवृद्धि
जन्मजात अधिवृक्क अतिवृद्धि है an inherited (genetic) condition causing swelling of the adrenal glands. The condition is associated with a decrease in the blood level of a hormone called cortisol and an increase in the level of male sex hormones (androgens) in both sexes. What is congenital adrenal hyperplasia. Congenital adrenal hyperplasia.
Patient information leaflet
एडिसन की बीमारी
Addison's disease is a condition in which your adrenal glands are not working as well as they should. In Addison's disease the adrenal glands do not produce as much of the steroid hormones (such as cortisol) as they normally do. Cancers of other parts of the body, which can spread and destroy the adrenals. Rare hereditary conditions - के लिए example,.
Patient information leaflet
ग्लाइकोजन भंडारण विकार
Glycogen storage disorders are a group of inherited diseases. Autosomal recessive inheritance pattern Most, but not all, glycogen storage disorders are inherited in a pattern called autosomal recessive inheritance. If both parents are carriers of the faulty gene, the chance of each one of their chi... X-लिंक्ड वंशानुक्रम पैटर्न This occurs in.
Patient information leaflet
स्टेरॉयड्स
Steroid medicines are used for many different medical conditions. Steroids can be given as creams/ointments (eg, for eczema or dermatitis), as a nasal spray (eg, for hay fever or ... How do steroids work. स्टेरॉयड्स are a man-made version of hormones normally produced by the adrenal glands, which are just above each kidney. When taken in doses.
Patient information leaflet
एक्रोमेगली
What causes acromegaly... In nearly everyone with acromegaly, the excess hormone comes from a small growth (tumour) in the pituitary gland (a pea-sized gland below the brain). This is a non-cancerous (benign) growth called a pituitary adenoma. As a result, the pituitary gland may stop being able to produce some other hormones. This can cause an.
Patient information leaflet
Low blood pressure
Low blood pressure (also called hypotension) is quite common and isn't usually a problem. However, it can cause symptoms in some people or some situations. This re... Diabetes over time can affect the sensors in the arteries especially after meals or when standing - which can lead to feeling dizzy or faint. Adrenal gland problems - eg, Addison's.
अधिक पठन और संदर्भ
- X-linked adrenal hypoplasia congenita; MedlinePlus, National Library of Medicine.
- Achermann JC, Vilain EJ. NR0B1-Related Adrenal Hypoplasia Congenita. 2001 Nov 20 [updated 2018 Jan 25]. In: Adam MP, Bick S, Mirzaa GM, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2026. Available from http://www.ncbi.nlm.nih.gov/books/NBK1431/
- Ahmad I, Paterson WF, Lin L, Adlard P, Duncan P, Tolmie J, Achermann JC, Donaldson MD. A novel missense mutation in DAX-1 with an unusual presentation of X-linked adrenal hypoplasia congenita. Horm Res. 2007;68(1):32-7. doi: 10.1159/000099835. Epub 2007 Feb 16.
- Choi HS, Kwon A, Chae HW, Suh J, Song KC, Lee JS, Kim HS. Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita. Ann Pediatr Endocrinol Metab. 2021 Jun;26(2):126-129. doi: 10.6065/apem.2040088.044. Epub 2021 Jun 30.
- Clipsham R, McCabe ER. DAX1 and its network partners: exploring complexity in development. Mol Genet Metab. 2003 Sep-Oct;80(1-2):81-120. doi: 10.1016/j.ymgme.2003.08.023.
- Fujieda K, Okuhara K, Abe S, Tajima T, Mukai T, Nakae J. Molecular pathogenesis of lipoid adrenal hyperplasia and adrenal hypoplasia congenita. J Steroid Biochem Mol Biol. 2003 Jun;85(2-5):483-9. doi: 10.1016/s0960-0760(03)00232-2.
- Fujieda K, Tajima T. Molecular basis of adrenal insufficiency. Pediatr Res. 2005 May;57(5 Pt 2):62R-69R. doi: 10.1203/01.PDR.0000159568.31749.4D. Epub 2005 Apr 6.
- Hammer GD, Parker KL, Schimmer BP. Minireview: transcriptional regulation of adrenocortical development. Endocrinology. 2005 Mar;146(3):1018-24. doi: 10.1210/en.2004-1385. Epub 2004 Dec 16.
- Lalli E, Sassone-Corsi P. DAX-1, an unusual orphan receptor at the crossroads of steroidogenic function and sexual differentiation. Mol Endocrinol. 2003 Aug;17(8):1445-53. doi: 10.1210/me.2003-0159. Epub 2003 May 29.
- Ludbrook LM, Harley VR. Sex determination: a 'window' of DAX1 activity. Trends Endocrinol Metab. 2004 Apr;15(3):116-21. doi: 10.1016/j.tem.2004.02.002.
- Mantovani G, De Menis E, Borretta G, Radetti G, Bondioni S, Spada A, Persani L, Beck-Peccoz P. DAX1 and X-linked adrenal hypoplasia congenita: clinical and molecular analysis in five patients. Eur J Endocrinol. 2006 May;154(5):685-9. doi: 10.1530/eje.1.02132.
- Sehgal A, Stack J. Complex glycerol kinase deficiency: an X-linked disorder associated with adrenal hypoplasia congenita. Indian J Pediatr. 2005 Jan;72(1):67-9. doi: 10.1007/BF02760584.
- Tabarin A. Congenital adrenal hypoplasia and DAX-1 gene mutations. Ann Endocrinol (Paris). 2001 Apr;62(2):202-6.
- Wikiera B, Jakubiak A, Laczmanska I, Noczynska A, Smigiel R. Complex glycerol kinase deficiency - long-term follow-up of two patients. Pediatr Endocrinol Diabetes Metab. 2021;27(3):227-231. doi: 10.5114/pedm.2021.109681.
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