SCROFULODERMA LEADING TO LYMPHEDEMA OF EXTERNAL GENITALIA AND LOWER EXTREMITIES Case Report

1977 ◽  
Vol 59 (3) ◽  
pp. 436-438 ◽  
Author(s):  
MALTI GUPTA ◽  
BALWANT S. CHANDALIA
2017 ◽  
Vol 32 (suppl_3) ◽  
pp. iii190-iii190
Author(s):  
Sibel Kocak ◽  
Arzu Ozdemir Kayalar ◽  
Fatih Akbay ◽  
Aysegul Kudu ◽  
Gunden Deger ◽  
...  

2011 ◽  
Vol 64 (1) ◽  
pp. 71
Author(s):  
Hee Jung Suh ◽  
Wan Tae Kim ◽  
Min Jeong Seo ◽  
Yoon Jung Kim

2012 ◽  
Vol 12 (1) ◽  
pp. 55 ◽  
Author(s):  
Senija Rašić ◽  
Jasminka Džemidžić ◽  
Zinaida Karasalihović ◽  
Vedad Herenda ◽  
Damir Rebić

2009 ◽  
Vol 62 (10) ◽  
pp. e401-e404 ◽  
Author(s):  
C. Rubino ◽  
A. Figus ◽  
M. Mazzocchi ◽  
L.A. Dessy ◽  
A. Martano

2021 ◽  
Vol 10 (1) ◽  
pp. 45-47
Author(s):  
Anil Kumar Sah ◽  
Bipin Maharjan ◽  
Mahesh Bahadur Adhikari ◽  
Suman Baral ◽  
Mimi Giri

Disorder of Sexual Development (DSD) is a group of congenital conditions with atypical development of sex at chromosomal, gonadal or anatomic level. Genetic males with DSD (46 XY DSD) can present with female external genital phenotype, ambiguous, or a micropenis. It is caused by incomplete intrauterine masculinization with or without the presence of Müllerian structures. It results either from decreased synthesis of testosterone or DHT or from impairment of androgen action. Herein, we report a case of a 13-year child raised as female with hoarseness of voice and gradual enlargement of clitoris with hormonal assessment not suggestive of either 5 Alfa Reductase deficiency, Congenital Adrenal Insufficiency Syndrome or 17β-Hydroxysteroid Dehydrogenase deficiency


1972 ◽  
Vol 7 (4) ◽  
pp. 477
Author(s):  
Chang Soo Kang ◽  
Ik Dong Kim ◽  
Young Sik Pyun ◽  
Yoon Soo Kim ◽  
Jong Sun Lim

Author(s):  
Tejal Kansara ◽  
Tushar Shah ◽  
Yesha Umbharatwala

Authors report a case of a 6-year-old child with syndromic 46, XY disorder of sexual development. From the birth patient was assigned female. Physical examination showed dysmorphic features and ambiguous external genitalia. Cytogenetic analysis of cultured peripheral blood lymphocytes revealed a male karyotype. The result of the chromosomal investigation showing male genetic sex, together with the ambivalent aspect of the external genitalia and gonads that are exclusively testes led to the diagnosis of 46, XY disorder of sexual development. The clinical management will help the child and the family deal effectively with this condition A multidisciplinary approach to this problem involving pediatricians, specialists in the field of endocrinology, genetics, surgery and psychiatry is necessary in order to reach a prompt and correct diagnosis and treatment.


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