Transsexual Symptoms in a Male Child Treated by a Female Therapist

Autoamputation of the appendix has previously been reported in the literature, but it is likely an unusual event. We report a 2-year-old male child who had previously undergone laparotomy and bowel resection for necrotizing enterocolitis. Two years later a calcified intra-abdominal mass was identified on abdominal radiography and ultrasonography. Eventual laparotomy revealed a densely calcified mass within the transverse mesocolon. The mass was uneventfully resected. Pathologic evaluation showed appendiceal tissue, consistent with prior autoamputation of the vermiform appendix. Autoamputation of the appendix has not to our knowledge previously been associated with a calcified mass nor been associated with a history of necrotizing enterocolitis, and these factors distinguish this case as noteworthy.

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Urethral Meatoplasty in the Male Child

Southern Medical Journal ◽

10.1097/00007611-196905000-00003 ◽

1969 ◽

Vol 62 (5) ◽

pp. 513

Author(s):

HOWARD M. RADWIN

Keyword(s):

Male Child

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Caroli Disease Associated With Vein of Galen Malformation in a Male Child

PEDIATRICS ◽

10.1542/peds.2013-0747 ◽

2014 ◽

Vol 134 (1) ◽

pp. e284-e288 ◽

Cited By ~ 2

Author(s):

D. Grieb ◽

A. Feldkamp ◽

T. Lang ◽

M. Melter ◽

C. Stroszczynski ◽

...

Keyword(s):

Male Child ◽

Vein Of Galen ◽

Vein Of Galen Malformation ◽

Caroli Disease

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The Child Buyer. A novel in the form of hearings before the Standing Committee on Education, Welfare, and Public Morality of a certain state Senate, investigating the conspiracy of Mr. Wissey Jones, with others, to purchase a male child. John Hersey. Knopf, New York, 1960. 257 pp. $4

Science ◽

10.1126/science.133.3452.573 ◽

1961 ◽

Vol 133 (3452) ◽

pp. 573-573

Author(s):

M. Mead

Keyword(s):

New York ◽

Male Child ◽

Public Morality ◽

Standing Committee ◽

State Senate

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A Case of Angelman Syndrome Arising as a Result of a De Novo Robertsonian Translocation

Acta geneticae medicae et gemellologiae twin research ◽

10.1017/s0001566000001410 ◽

1996 ◽

Vol 45 (1-2) ◽

pp. 255-261 ◽

Cited By ~ 3

Author(s):

S. Ramsden ◽

L. Gaunt ◽

A. Seres-Santamaria ◽

J. Clayton-Smith

Keyword(s):

Angelman Syndrome ◽

Robertsonian Translocation ◽

De Novo ◽

Uniparental Disomy ◽

Male Child ◽

Paternal Uniparental Disomy

AbstractA male child has been identified with Angelman syndrome. He has been shown to carry a de novo Robertsonian 15/15 translocation where both chromosome 15s have been derived from the father. Consequently the disease in this instance is due to paternal uniparental disomy.

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