A RARE CASE OF NON-CLASSICAL TYPE OF CONGENITAL ADRENAL HYPERPLASIA IN A 27-YEAR-OLD FEMALE
This case report presents the case of a 27-year-old female patient with a complex clinical presentation, diagnosed with nonclassical congenital adrenal hyperplasia (NCCAH). The patient presented with a constellation of symptoms including hirsutism, acne, hyperpigmentation, amenorrhea, frontal baldne...
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Veröffentlicht in: | Journal of Ayub Medical College, Abbottabad Abbottabad, 2024-04, Vol.36 (2), p.436-438 |
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creator | Ali, Masab Ahmad, Muhammad Husnain Mirza, Zaid Ashraf |
description | This case report presents the case of a 27-year-old female patient with a complex clinical presentation, diagnosed with nonclassical congenital adrenal hyperplasia (NCCAH). The patient presented with a constellation of symptoms including hirsutism, acne, hyperpigmentation, amenorrhea, frontal baldness, and renal stones, posing diagnostic challenges. Comprehensive evaluation revealed NCCAH, emphasizing the importance of considering this condition in cases of hyperandrogenism. Treatment with oral dexamethasone and oral contraceptive pills resulted in gradual symptom improvement. This case underscores the necessity for thorough clinical assessment and awareness of NCCAH as a differential diagnosis in patients with hyperandrogenic symptoms. |
doi_str_mv | 10.55519/JAMC-02-12419 |
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The patient presented with a constellation of symptoms including hirsutism, acne, hyperpigmentation, amenorrhea, frontal baldness, and renal stones, posing diagnostic challenges. Comprehensive evaluation revealed NCCAH, emphasizing the importance of considering this condition in cases of hyperandrogenism. Treatment with oral dexamethasone and oral contraceptive pills resulted in gradual symptom improvement. This case underscores the necessity for thorough clinical assessment and awareness of NCCAH as a differential diagnosis in patients with hyperandrogenic symptoms.</description><identifier>ISSN: 1025-9589</identifier><identifier>EISSN: 1819-2718</identifier><identifier>DOI: 10.55519/JAMC-02-12419</identifier><identifier>PMID: 39609997</identifier><language>eng</language><publisher>Pakistan</publisher><subject>Adrenal Hyperplasia, Congenital - complications ; Adrenal Hyperplasia, Congenital - diagnosis ; Adrenal Hyperplasia, Congenital - drug therapy ; Adult ; Amenorrhea - etiology ; Dexamethasone - therapeutic use ; Diagnosis, Differential ; Female ; Hirsutism - diagnosis ; Hirsutism - etiology ; Humans ; Hyperandrogenism - diagnosis ; Hyperandrogenism - etiology ; Hyperpigmentation - diagnosis ; Kidney Calculi - diagnosis</subject><ispartof>Journal of Ayub Medical College, Abbottabad, 2024-04, Vol.36 (2), p.436-438</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0009-0006-5248-0749</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39609997$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ali, Masab</creatorcontrib><creatorcontrib>Ahmad, Muhammad Husnain</creatorcontrib><creatorcontrib>Mirza, Zaid Ashraf</creatorcontrib><title>A RARE CASE OF NON-CLASSICAL TYPE OF CONGENITAL ADRENAL HYPERPLASIA IN A 27-YEAR-OLD FEMALE</title><title>Journal of Ayub Medical College, Abbottabad</title><addtitle>J Ayub Med Coll Abbottabad</addtitle><description>This case report presents the case of a 27-year-old female patient with a complex clinical presentation, diagnosed with nonclassical congenital adrenal hyperplasia (NCCAH). The patient presented with a constellation of symptoms including hirsutism, acne, hyperpigmentation, amenorrhea, frontal baldness, and renal stones, posing diagnostic challenges. Comprehensive evaluation revealed NCCAH, emphasizing the importance of considering this condition in cases of hyperandrogenism. Treatment with oral dexamethasone and oral contraceptive pills resulted in gradual symptom improvement. This case underscores the necessity for thorough clinical assessment and awareness of NCCAH as a differential diagnosis in patients with hyperandrogenic symptoms.</description><subject>Adrenal Hyperplasia, Congenital - complications</subject><subject>Adrenal Hyperplasia, Congenital - diagnosis</subject><subject>Adrenal Hyperplasia, Congenital - drug therapy</subject><subject>Adult</subject><subject>Amenorrhea - etiology</subject><subject>Dexamethasone - therapeutic use</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Hirsutism - diagnosis</subject><subject>Hirsutism - etiology</subject><subject>Humans</subject><subject>Hyperandrogenism - diagnosis</subject><subject>Hyperandrogenism - etiology</subject><subject>Hyperpigmentation - diagnosis</subject><subject>Kidney Calculi - diagnosis</subject><issn>1025-9589</issn><issn>1819-2718</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kDFPwzAUhC0EoqWwMiL_ARc_O3byRit12qA0qdIsFUPk1IkEoqJKxMC_J22B6Z7u3d3wEfIIfK6UAnx-MeuYccFABIBXZAoRIBMhRNfjzYViqCKckLtheOdcChnxWzKRqDkihlPyamhpSktjs7W0SGhe5CzOzHabxiaj1W5zduMiX9o8rUbLLEqbj7oaX-VmTKaGpjk1VIRsZ03JimxBE7s2mb0nN537GNqHX52RKrFVvGJZsTzNsz2qkKEOtEdAJXQXNKC5BK0ECK28dg78njvVhh6CwLuuUY2QHjx6FzQNSD3GZ2R-md33n8PQt1197N8Orv-ugddnSPUJUs1FfYY0Fp4uheNXc2j9f_yPivwBngVYSA</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Ali, Masab</creator><creator>Ahmad, Muhammad Husnain</creator><creator>Mirza, Zaid Ashraf</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0009-0006-5248-0749</orcidid></search><sort><creationdate>202404</creationdate><title>A RARE CASE OF NON-CLASSICAL TYPE OF CONGENITAL ADRENAL HYPERPLASIA IN A 27-YEAR-OLD FEMALE</title><author>Ali, Masab ; Ahmad, Muhammad Husnain ; Mirza, Zaid Ashraf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c957-9646d919526f4b160316521265d6aa1dc0a5e7d144dafb5b23d1d9da4bb136603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adrenal Hyperplasia, Congenital - complications</topic><topic>Adrenal Hyperplasia, Congenital - diagnosis</topic><topic>Adrenal Hyperplasia, Congenital - drug therapy</topic><topic>Adult</topic><topic>Amenorrhea - etiology</topic><topic>Dexamethasone - therapeutic use</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Hirsutism - diagnosis</topic><topic>Hirsutism - etiology</topic><topic>Humans</topic><topic>Hyperandrogenism - diagnosis</topic><topic>Hyperandrogenism - etiology</topic><topic>Hyperpigmentation - diagnosis</topic><topic>Kidney Calculi - diagnosis</topic><toplevel>online_resources</toplevel><creatorcontrib>Ali, Masab</creatorcontrib><creatorcontrib>Ahmad, Muhammad Husnain</creatorcontrib><creatorcontrib>Mirza, Zaid Ashraf</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of Ayub Medical College, Abbottabad</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ali, Masab</au><au>Ahmad, Muhammad Husnain</au><au>Mirza, Zaid Ashraf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A RARE CASE OF NON-CLASSICAL TYPE OF CONGENITAL ADRENAL HYPERPLASIA IN A 27-YEAR-OLD FEMALE</atitle><jtitle>Journal of Ayub Medical College, Abbottabad</jtitle><addtitle>J Ayub Med Coll Abbottabad</addtitle><date>2024-04</date><risdate>2024</risdate><volume>36</volume><issue>2</issue><spage>436</spage><epage>438</epage><pages>436-438</pages><issn>1025-9589</issn><eissn>1819-2718</eissn><abstract>This case report presents the case of a 27-year-old female patient with a complex clinical presentation, diagnosed with nonclassical congenital adrenal hyperplasia (NCCAH). The patient presented with a constellation of symptoms including hirsutism, acne, hyperpigmentation, amenorrhea, frontal baldness, and renal stones, posing diagnostic challenges. Comprehensive evaluation revealed NCCAH, emphasizing the importance of considering this condition in cases of hyperandrogenism. Treatment with oral dexamethasone and oral contraceptive pills resulted in gradual symptom improvement. This case underscores the necessity for thorough clinical assessment and awareness of NCCAH as a differential diagnosis in patients with hyperandrogenic symptoms.</abstract><cop>Pakistan</cop><pmid>39609997</pmid><doi>10.55519/JAMC-02-12419</doi><tpages>3</tpages><orcidid>https://orcid.org/0009-0006-5248-0749</orcidid></addata></record> |
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subjects | Adrenal Hyperplasia, Congenital - complications Adrenal Hyperplasia, Congenital - diagnosis Adrenal Hyperplasia, Congenital - drug therapy Adult Amenorrhea - etiology Dexamethasone - therapeutic use Diagnosis, Differential Female Hirsutism - diagnosis Hirsutism - etiology Humans Hyperandrogenism - diagnosis Hyperandrogenism - etiology Hyperpigmentation - diagnosis Kidney Calculi - diagnosis |
title | A RARE CASE OF NON-CLASSICAL TYPE OF CONGENITAL ADRENAL HYPERPLASIA IN A 27-YEAR-OLD FEMALE |
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