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}}'''Late onset congenital adrenal hyperplasia''' (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of [[congenital adrenal hyperplasia]] (CAH)<ref name=":0">{{Cite journal |last=Adriaansen |first=Bas P. H. |last2=Schröder |first2=Mariska A. M. |last3=Span |first3=Paul N. |last4=Sweep |first4=Fred C. G. J. |last5=van Herwaarden |first5=Antonius E. |last6=Claahsen-van der Grinten |first6=Hedi L. |date=2022-12-12 |title=Challenges in treatment of patients with non-classic congenital adrenal hyperplasia |url=https://www.frontiersin.org/articles/10.3389/fendo.2022.1064024/full |journal=Frontiers in Endocrinology |volume=13 |pages=1064024 |doi=10.3389/fendo.2022.1064024 |issn=1664-2392 |pmc=PMC9791115 |pmid=36578966}}</ref>, a group of [[Genetic disorder#Autosomal recessive|autosomal recessive disorders]] characterized by impaired [[cortisol]] synthesis that leads to variable degrees of [[Postpartum period|postnatal]] [[androgen]] excess<ref name=":0" /><ref name="pmid30272171">{{cite journal | vauthors = Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC | display-authors = 6 | title = Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 103 | issue = 11 | pages = 4043–4088 | date = November 2018 | pmid = 30272171 | pmc = 6456929 | doi = 10.1210/jc.2018-01865 }}</ref><ref name="pmid7951484">{{cite journal | vauthors = Hattori N, Ishihara T, Moridera K, Hino M, Ikekubo K, Kurahachi H | title = A case of late-onset congenital adrenal hyperplasia due to partial 3 beta-hydroxysteroid dehydrogenase deficiency | journal = Endocrine Journal | volume = 40 | issue = 1 | pages = 107–9 | date = February 1993 | pmid = 7951484 | doi = 10.1507/endocrj.40.107 | url = https://www.jstage.jst.go.jp/article/endocrj1993/40/1/40_1_107/_article | doi-access = free }}</ref><ref name="omim202010">{{Cite web|url=https://www.omim.org/entry/202010|title=OMIM Entry - # 202010 - ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY|website=www.omim.org}}</ref>.
}}'''Late onset congenital adrenal hyperplasia''' (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of [[congenital adrenal hyperplasia]] (CAH)<ref name=":0">{{Cite journal |last=Adriaansen |first=Bas P. H. |last2=Schröder |first2=Mariska A. M. |last3=Span |first3=Paul N. |last4=Sweep |first4=Fred C. G. J. |last5=van Herwaarden |first5=Antonius E. |last6=Claahsen-van der Grinten |first6=Hedi L. |date=2022-12-12 |title=Challenges in treatment of patients with non-classic congenital adrenal hyperplasia |url=https://www.frontiersin.org/articles/10.3389/fendo.2022.1064024/full |journal=Frontiers in Endocrinology |volume=13 |pages=1064024 |doi=10.3389/fendo.2022.1064024 |issn=1664-2392 |pmc=9791115 |pmid=36578966}}</ref>, a group of [[Genetic disorder#Autosomal recessive|autosomal recessive disorders]] characterized by impaired [[cortisol]] synthesis that leads to variable degrees of [[Postpartum period|postnatal]] [[androgen]] excess<ref name=":0" /><ref name="pmid30272171">{{cite journal | vauthors = Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC | display-authors = 6 | title = Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 103 | issue = 11 | pages = 4043–4088 | date = November 2018 | pmid = 30272171 | pmc = 6456929 | doi = 10.1210/jc.2018-01865 }}</ref><ref name="pmid7951484">{{cite journal | vauthors = Hattori N, Ishihara T, Moridera K, Hino M, Ikekubo K, Kurahachi H | title = A case of late-onset congenital adrenal hyperplasia due to partial 3 beta-hydroxysteroid dehydrogenase deficiency | journal = Endocrine Journal | volume = 40 | issue = 1 | pages = 107–9 | date = February 1993 | pmid = 7951484 | doi = 10.1507/endocrj.40.107 | url = https://www.jstage.jst.go.jp/article/endocrj1993/40/1/40_1_107/_article | doi-access = free }}</ref><ref name="omim202010">{{Cite web|url=https://www.omim.org/entry/202010|title=OMIM Entry - # 202010 - ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY|website=www.omim.org}}</ref>.


The causes of LOCAH are the same as of [[Congenital adrenal hyperplasia#Classic|classic CAH]], and in the majority of the cases are the [[mutation]]s in the ''[[CYP21A2]]'' gene resulting in corresponding activity changes in the associated [[21-Hydroxylase|P450c21 (21-hydroxylase)]] [[enzyme]] which ultimately leads to excessive [[androgen]] production. Other causes, albeit less frequent, are mutations in genes affecting other enzymes involved in [[steroid]] [[metabolism]], like [[Steroid 11β-hydroxylase|11β-hydroxylase]] or [[3β-hydroxysteroid dehydrogenase]]. It has a prevalence between 0.1% and 2% depending on population,<ref name="pmid30272171"/> and is one of the most common autosomal recessive genetic diseases in humans.<ref name="pmid9556656">{{cite journal | vauthors = Speiser PW, Dupont B, Rubinstein P, Piazza A, Kastelan A, New MI | title = High frequency of nonclassical steroid 21-hydroxylase deficiency | journal = American Journal of Human Genetics | volume = 37 | issue = 4 | pages = 650–67 | date = July 1985 | pmid = 9556656 | pmc = 1684620 }}</ref><ref name="pmid19500762">{{cite journal | vauthors = Krone N, Arlt W | title = Genetics of congenital adrenal hyperplasia | journal = Best Practice & Research. Clinical Endocrinology & Metabolism | volume = 23 | issue = 2 | pages = 181–92 | date = April 2009 | pmid = 19500762 | pmc = 5576025 | doi = 10.1016/j.beem.2008.10.014 }}</ref><ref name="pmid26865584">{{cite journal | vauthors = Turcu AF, Nanba AT, Chomic R, Upadhyay SK, Giordano TJ, Shields JJ, Merke DP, Rainey WE, Auchus RJ | display-authors = 6 | title = Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency | journal = European Journal of Endocrinology | volume = 174 | issue = 5 | pages = 601–9 | date = May 2016 | pmid = 26865584 | pmc = 4874183 | doi = 10.1530/EJE-15-1181 }}</ref> The pathophysiology is complex and not all individuals are symptomatic.<ref name="pmid30272171"/>
The causes of LOCAH are the same as of [[Congenital adrenal hyperplasia#Classic|classic CAH]], and in the majority of the cases are the [[mutation]]s in the ''[[CYP21A2]]'' gene resulting in corresponding activity changes in the associated [[21-Hydroxylase|P450c21 (21-hydroxylase)]] [[enzyme]] which ultimately leads to excessive [[androgen]] production. Other causes, albeit less frequent, are mutations in genes affecting other enzymes involved in [[steroid]] [[metabolism]], like [[Steroid 11β-hydroxylase|11β-hydroxylase]] or [[3β-hydroxysteroid dehydrogenase]]. It has a prevalence between 0.1% and 2% depending on population,<ref name="pmid30272171"/> and is one of the most common autosomal recessive genetic diseases in humans.<ref name="pmid9556656">{{cite journal | vauthors = Speiser PW, Dupont B, Rubinstein P, Piazza A, Kastelan A, New MI | title = High frequency of nonclassical steroid 21-hydroxylase deficiency | journal = American Journal of Human Genetics | volume = 37 | issue = 4 | pages = 650–67 | date = July 1985 | pmid = 9556656 | pmc = 1684620 }}</ref><ref name="pmid19500762">{{cite journal | vauthors = Krone N, Arlt W | title = Genetics of congenital adrenal hyperplasia | journal = Best Practice & Research. Clinical Endocrinology & Metabolism | volume = 23 | issue = 2 | pages = 181–92 | date = April 2009 | pmid = 19500762 | pmc = 5576025 | doi = 10.1016/j.beem.2008.10.014 }}</ref><ref name="pmid26865584">{{cite journal | vauthors = Turcu AF, Nanba AT, Chomic R, Upadhyay SK, Giordano TJ, Shields JJ, Merke DP, Rainey WE, Auchus RJ | display-authors = 6 | title = Adrenal-derived 11-oxygenated 19-carbon steroids are the dominant androgens in classic 21-hydroxylase deficiency | journal = European Journal of Endocrinology | volume = 174 | issue = 5 | pages = 601–9 | date = May 2016 | pmid = 26865584 | pmc = 4874183 | doi = 10.1530/EJE-15-1181 }}</ref> The pathophysiology is complex and not all individuals are symptomatic.<ref name="pmid30272171"/>

Revision as of 12:38, 13 April 2023

Late onset congenital adrenal hyperplasia
Other namesNonclassic onset congenital adrenal hyperplasia
Frequency0.1%–2%

Late onset congenital adrenal hyperplasia (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of congenital adrenal hyperplasia (CAH)[1], a group of autosomal recessive disorders characterized by impaired cortisol synthesis that leads to variable degrees of postnatal androgen excess[1][2][3][4].

The causes of LOCAH are the same as of classic CAH, and in the majority of the cases are the mutations in the CYP21A2 gene resulting in corresponding activity changes in the associated P450c21 (21-hydroxylase) enzyme which ultimately leads to excessive androgen production. Other causes, albeit less frequent, are mutations in genes affecting other enzymes involved in steroid metabolism, like 11β-hydroxylase or 3β-hydroxysteroid dehydrogenase. It has a prevalence between 0.1% and 2% depending on population,[2] and is one of the most common autosomal recessive genetic diseases in humans.[5][6][7] The pathophysiology is complex and not all individuals are symptomatic.[2]

Presentation

Patients with LOCAH usually present with signs of hyperandrogenism, rather than of glucocorticoid deficiency, a condition characterized by inadequate cortisol production.[8][9] Cortisol synthesis impairment is mild but clinically silent.[10] LOCAH patients usually have the same baseline but lower peak cortisol levels comparing to healthy controls.[11][12] Flatter diurnal cortisol slopes contribute to stress-related dysregulation of central and peripheral circadian mechanisms with negative health outcomes.[13][14][15]

Due to hyperandrogenism, females may present with symptoms like hirsutism, oligomenorrhea, acne, infertility,[16] and male-pattern baldness.[17][18][19]

Males are generally asymptomatic,[20][8] but may present with acne,[21][22][23] early balding,[24][25][26] chronic prostatitis, chronic pelvic pain syndrome,[27][28][29] and very rarely, testicular adrenal rest tumors.[30][16][24]

While symptoms are usually diagnosed after puberty, children may present with premature adrenarche.[8]

The degree of hormonal disorder in patients with LOCAH is relatively mild. However, alterations in the hypothalamic–pituitary–adrenal axis are present even in this mild form of the disease and might contribute to psychiatric vulnerability.[10]

Molecular genetics

LOCAH is most commonly attributed to mutations in the CYP21A2 gene, which encodes the 21-hydroxylase enzyme. Cases of LOCAH due to deficiencies in other enzymes that are known causes of CAH (3β-hydroxysteroid dehydrogenase, steroid 11β-hydroxylase, etc.) are rare and have no established prevalence estimates.[31]

Several severe mutations have been associated with LOCAH: the deletion of the CYP21A2 gene, small gene conversions, the p. I172N (rs6475, c.518T>A, CYP21A2*11) mutation, the c.293-13A/C>G (rs6467, CYP21A2*9) mutation, and the p.Gln318Stop (p.Q318X, rs7755898, c.952C>T, CYP21A2*17) mutation.[32] Besides that, LOCAH due to 21-hydroxylase deficiency can be caused by duplications of CYP21A1P pseudogene and C4B gene. Due to the high degree of homology between the CYP21A2 gene and the CYP21A1P pseudogene, and the complexity of the locus, research on the sequencing level can be difficult.[33] A 2021 study showed that mild genotypes associated with LOCAH have a low concordance rate with those phenotypes, probably due to the complex characteristics of 21-hydroxylase genotyping and the limitation of using massive parallel sequencing alone without combining with other comprehensive methods.[34]

The following three mutations to the CYP21A2 gene have been found to result in a moderate reduction in enzyme activity associated with that allele (20–60% residual activity),[32] and are associated with LOCAH:[35]

  • p.V281L (rs6471, c.844G>C, CYP21A2*15);
  • p.P453S (rs6445, c.1360C>T, CYP21A2*19);
  • p.P30L (rs9378251, c.92C>T, CYP21A2*8).

A point mutation in exon 7 of CYP21A2, (p.V281L), is commonly found in LOCAH-associated alleles.[35][33][32] Carriers for this mutation retain 20%–50% of 21-hydroxylase activity,[36][20] but are at higher risk of symptoms of androgen excess than carriers of the severe mutations and had higher adrenocorticotropic hormone (ACTH) stimulated 17α-hydroxyprogesterone,[37] suggesting heterozygous mutations on CYP21A2 play an important role in disease.[38]

The particularly mild clinical symptoms of LOCAH such as hyperandrogenism, hirsutism and acne or infertility overlap with other diseases such as polycystic ovary syndrome. Biochemical parameters like 17α-hydroxyprogesterone may not be elevated in very mild cases of LOCAH, and may vary between labs that makes interpretation difficult. It may not be possible to perform ACTH stimulation tests in all institutions, depending on the availability of the injectable adrenocorticotropic hormone medication. This is why a comprehensive CYP21A2 genotyping (rather than variant-specific assays alone) is a good way to exclude/confirm 21-hydroxylase deficiency and heterozygosity (carrier) status.[39] Genetic testing can be used to exclude false positive diagnosis based on biochemical parameters alone, even with ACTH stimulation, since elevated 17-OHP levels may be also caused by ovarian or adrenal tumors, rather than by the variants in the CYP21A2 gene.[40]

Diagnosis

Originally characterized in 1957 by French biochemist Jacques Decourt,[41] LOCAH differs from classic CAH in that it does not cause atypical neonatal genital morphology, is not life-threatening and presents after birth. Unlike classic CAH, LOCAH generally cannot be reliably detected with neonatal screening.[42] Many individuals (both male and female) present no symptoms during childhood and adolescence and only become aware of the possibility of LOCAH due to the diagnosis of another family member. It is thought that 90% of women with LOCAH never receive a diagnosis.[10] In young females, premature pubarche is generally the first symptom to present.[18] The earliest known diagnosis was in a 6 month old female who developed pubic hair.[43] Additional symptoms include acne, menstrual irregularities and hirsutism in females as well as alopecia in males. LOCAH is often misdiagnosed as polycystic ovarian disease (PCOS).[44]

LOCAH is often diagnosed in the context of infertility assessment in women. During the follicular phase of the menstrual cycle, progesterone accumulates along with 17α-hydroxyprogesterone which can thin the endometrium and change cervical mucus in a manner similar to the effect of progestogen contraceptives, interferes with the normal menstrual cycle, which can lead to oligomenorrhea or amenorrhea[10] and impairs sperm penetration.[45] Abnormal endometrial development leads to decreased uterine receptivity, which also contributes to infertility.[46] Once attempting to conceive, most women with LOCAH will become pregnant within a year with or without treatment, but women with LOCAH have an increased risk of miscarriage.[10]

The diagnostic procedure varies according to the specific enzyme deficiency causing LOCAH and the precise serum androgen levels required for diagnosis are the subject to variance from different measurement methods, refinement in specific cases and are under active research. Some protocols are based on measuring 17α-hydroxyprogesterone levels, with or without ACTH stimulation test.[42][47]

21-Hydroxylase deficiency

Screening

Main article: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The condition of 21-hydroxylase deficiency is screened by measuring serum levels of 17α-hydroxyprogesterone (17-OHP) in the morning and between day 3 and 5 of the menstrual cycle (for females) to reduce the possibility of false positive results.[10] 17-OHP is used as a marker of the 21-hydroxylase enzyme activity since the 1980s.[48] The cutoff basal 17-OHP value is matter of debate.[20] Most commonly, the value of 2.0 ng/mL[2][49] is used, but a value of 1.7 ng/mL provides better selectivity.[20][42] Most research on the biochemical diagnosis of LOCAH relied on direct immunoassays, such as radioimmunoassays or time-resolved fluorescence assay to measure 17-OHP, therefore, cross-reactivity and reliability problems of these methods might have caused differences in the 17-OHP cutoff values recommended, so the use of liquid chromatography–mass spectrometry aims to improve the accuracy of 17-OHP measurement and increase diagnostic quality of LOCAH.[20] Randomly timed measurements of 17-OHP have not been shown to be useful for screening since they are often normal and are known to be very high in the luteal phase of the female menstrual cycle. After basal levels have been measured, confirmation is done by administering ACTH, and comparing 17-OHP pre and post test. 17-OHP levels over 10 ng/mL at the 60th minute post stimulation is considered diagnostic for LOCAH.[42]

Androgen backdoor pathway

Main article: Androgen backdoor pathway

In 21-hydroxylase deficiency, especially in mild cases (LOCAH), the androgen "backdoor" pathway may be the reason of androgen excess.[50] This backdoor pathway is not always considered in the clinical evaluation of patients with hyperandrogenism conditions such as LOCAH and may be a source of diagnostic pitfalls and confusion.[51] One case study demonstrated the importance of considering serum 5α-dihydrotestosterone (DHT) levels and the androgen backdoor pathway in a LOCAH diagnosis that would have not been apparent from testosterone levels alone.[51]

11β-Hydroxylase deficiency

Main article: Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

The activity of 11β-hydroxylase can be determined by observing the basal 11-deoxycortisol level. A level over 10 ng/mL, indicates followup with ACTH stimulation test. The 60th minute post-stimulation 11-deoxycortisol levels higher than 18 ng/mL are diagnostic of LOCAH.[42]

3β-Hydroxysteroid dehydrogenase deficiency

Main article: Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency

The activity of 3β-hydroxysteroid dehydrogenase can be determined by observing the basal 17α-hydroxypregnenolone level. A level above 30 ng/mL and 17α-hydroxypregnenolone/cortisol ratio above 10 SD are diagnostic of LOCAH.[42]

Management

Management and treatment of LOCAH is case specific[1] and the application of glucocorticoid treatment is not standard as it is in classic CAH[1]. LOCAH is not a life-threatening medical condition and the risks of treatment given prenatally or to asymptomatic children outweigh potential benefits.[52][53][54] In appropriate cases, glucocorticoids (usually hydrocortisone in children) are administered to suppress secretion of corticotropin releasing hormone (CRH) produced by hypothalamus and of adrenocorticotropic hormone (ACTH) produced by pituitary gland. This suppression will reduce concentration in blood of sex steroids produced by adrenal glands[1]. Some of the main considerations in treatment include the watchful waiting of symptom severity as well as adverse responses to glucocorticoids administered as drugs, seen in patient bone mineral density, height and weight[1].For women, an oral contraceptive pill and androgen blockers such as spironolactone or cyproterone acetate are alternatives to glucocorticoids for managing symptoms of androgen excess[1].There is still debate whether miscarriage rates in women with LOCAH are influenced by hydrocortisone treatment[1].

Prevalence

According to haplotype association studies, the prevalence of LOCAH in the general white population is estimated to be 1:500 to 1:1000, but in people with a high rate of marriage between relatives, the prevalence rate is as high as 1:50 to 1:100. A 2017 CYP21A2 genotype analysis predicted that the total frequency of LOCAH in the white population of the United States is about 1:200 (95% confidence level, from 1:100 to 1:280).[2][55]

According to a 2017 meta-analysis, the prevalence of LOCAH among women with signs and symptoms of androgen excess is 4.2% globally, and between 1% and 10% depending on the ethnicity of the population being studied.[20]

Anne Fausto-Sterling, an American sexologist, in a 2000 book "Sexing the Body" came up with an estimate that people with intersex conditions account for 1.7% of the general population.[56] This estimate is cited by a number of prominent intersex advocacy organizations.[57][58][59][60] Of these intersex individuals, according to Fausto-Sterling, 88% have LOCAH.[56] Leonard Sax, an American psychologist and a family physician, criticized these figures in a review published in 2002 in The Journal of Sex Research, stating that from the clinician's perspective, LOCAH is not an intersex condition.[61] Including LOCAH in intersex prevalence estimates has been cited as an example of misleading statistical practice.[62]

See also

References

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  52. ^ Miller WL, Witchel SF (May 2013). "Prenatal treatment of congenital adrenal hyperplasia: risks outweigh benefits". American Journal of Obstetrics and Gynecology. 208 (5): 354–9. doi:10.1016/j.ajog.2012.10.885. PMID 23123167.
  53. ^ Clayton PE, Miller WL, Oberfield SE, Ritzén EM, Sippell WG, Speiser PW (2002). "Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society". Hormone Research. 58 (4): 188–95. doi:10.1159/000065490. PMID 12324718. S2CID 41346214.
  54. ^ Joint LWPES/ESPE CAH Working Group (September 2002). "Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology". The Journal of Clinical Endocrinology and Metabolism. 87 (9): 4048–53. doi:10.1210/jc.2002-020611. PMID 12213842.
  55. ^ Hannah-Shmouni F, Morissette R, Sinaii N, Elman M, Prezant TR, Chen W, et al. (November 2017). "Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians". Genetics in Medicine. 19 (11): 1276–1279. doi:10.1038/gim.2017.46. PMC 5675788. PMID 28541281. S2CID 4630175.
  56. ^ a b Fausto-Sterling A (30 November 2000). Sexing the body : gender politics and the construction of sexuality. [New York]. ISBN 9780465077137.{{cite book}}: CS1 maint: location missing publisher (link)
  57. ^ "Intersex babies are perfect just as they are!". UN Free & Equal. up to 1.7 percent of babies are born with sex characteristics that don't fit typical definitions of male and female. That makes being intersex almost as common as being a redhead!
  58. ^ "Its Intersex Awareness Day - here are 5 myths we need to shatter". www.amnesty.org. 26 October 2018. According to experts, around 1.7% of the population is born with intersex traits - comparable to the number of people born with red hair.
  59. ^ "What is Intersex? Frequently Asked Questions". interACT: Advocates for Intersex Youth. About 1.7% of people are born intersex. (Compare that to a ~0.3% chance of having identical twins!) 1 in 2,000 babies (0.05% of humans) are born with genital differences that a doctor might suggest changing with unnecessary surgery.
  60. ^ "Intersex population figures". Intersex Human Rights Australia. 28 September 2013. Given that intersex people only come to the attention of data collectors through chance or an apparent medical reason, the actual numbers of people with intersex variations are likely to be as much as 1.7%. Despite the limitations of the data, 1.7% seems more justifiable as an upper limit figure than alternatives, to date.
  61. ^ Sax L (August 2002). "How common is intersex? a response to Anne Fausto-Sterling". Journal of Sex Research. 39 (3): 174–8. doi:10.1080/00224490209552139. PMID 12476264. S2CID 33795209. Reviewing the list of conditions which Fausto-Sterling considers to be intersex, we find that this one condition–late-onset congenital adrenal hyperplasia (LOCAH)–accounts for 88% of all those patients whom Fausto-Sterling classifies as intersex (1.5/1.7 = 88%). From a clinician's perspective, however, LOCAH is not an intersex condition. The genitalia of these babies are normal at birth, and consonant with their chromosomes: XY males have normal male genitalia, and XX females have normal female genitalia.
  62. ^ Best J (14 September 2013). Stat-spotting : a field guide to identifying dubious data (Updated and expand ed.). Berkeley. pp. 12–13. ISBN 978-0520279988.{{cite book}}: CS1 maint: location missing publisher (link)
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