Galactocele in a Male Infant: Case Report and Review of Literature

1993 ◽  
Vol 13 (3) ◽  
pp. 305-308 ◽  
Author(s):  
M. Boyle ◽  
K. Lakhoo ◽  
P. Ramani
Keyword(s):  
Case Report ◽  
Male Infant ◽  
Review Of Literature ◽  
Infant Case

Solitary mastocytoma in an infant — case report with review of literature

2000 ◽  
Vol 52 (1) ◽  
pp. 93-95 ◽  
Author(s):  
Ashutosh Kacker ◽  
Jerry Huo ◽  
Ruoqing Huang ◽  
Rana S Hoda
Keyword(s):  
Case Report ◽  
Review Of Literature ◽  
Infant Case ◽  
Solitary Mastocytoma

Lemierre syndrome in a 5-month-old male infant: Case report and review of the pediatric literature

2008 ◽  
Vol 9 (5) ◽  
pp. e35-e37 ◽  
Author(s):  
François Aspesberro ◽  
Thomas Siebler ◽  
Jean-Paul Van Nieuwenhuyse ◽  
Eugène Panosetti ◽  
Françoise Berthet
Keyword(s):  
Case Report ◽  
Male Infant ◽  
Lemierre Syndrome ◽  
Infant Case

scholarly journals Piebaldism in a 3-month-old infant: Case report

2014 ◽  
Vol 67 (3-4) ◽  
pp. 109-110
Author(s):  
Olgica Milankov ◽  
Radojica Savic ◽  
Anica Radulovic
Keyword(s):  
Case Report ◽  
Family History ◽  
Autosomal Dominant ◽  
Male Infant ◽  
Congenital Absence ◽  
Skin Involvement ◽  
Left Forearm ◽  
Autosomal Dominant Disorder ◽  
And Migration ◽  
Infant Case

Introduction. Piebaldism is an autosomal dominant disorder characterized by the congenital absence of melanocytes in the affected areas of skin and hair due to mutations of the KIT protooncogene, which affects the differentiation and migration of melanoblasts. Case report. A 3 ? month old male infant was admitted to hospital due to depigmentation of skin in the area of forehead, trunk and extremities. On admission, he had multiple, irregularly shaped areas of leucoderma present at the forehead, abdomen, lower legs and left forearm. Based on the characteristic skin features and family history, we diagnosed the boy?s leucoderma as piebaldism. Conclusion. Vitiligo differs from piebaldism by the presence of unstable hypopigmented lesions that are acquired later in life. Albinism presents with widespread skin involvement and lacks the characteristic hyperpigmented macules within hypopigmented areas.

Osteoskeletal Manifestation of Scurvy in a Male Infant (Case Report)

2008 ◽  
Vol 1 (1) ◽  
pp. 64-67 ◽  
Author(s):  
Nada Pop-Jordanova ◽  
Nevenka Slavevska ◽  
Stojka Fustic
Keyword(s):  
Case Report ◽  
Male Infant ◽  
Infant Case

Hair Follicle Nevus Located on the Chin of an Infant: Case Report and Review of Literature

2016 ◽  
Vol 33 (2) ◽  
pp. e106-e108 ◽  
Author(s):  
Krista N. Larson ◽  
Patrick O'Shea ◽  
Daniel C. Zedek ◽  
Dean S. Morrell
Keyword(s):  
Case Report ◽  
Hair Follicle ◽  
Review Of Literature ◽  
Infant Case

Concomitant Congenital Horner and Harlequin Syndromes: Case Report and Review of Literature

2020 ◽  
Author(s):  
Ayman G. Elnahry ◽  
Aisha A. Gamal Eldin ◽  
Aya G. Elnahry ◽  
Gehad A. Elnahry
Keyword(s):  
Case Report ◽  
Autonomic Dysfunction ◽  
Rare Case ◽  
Rare Condition ◽  
Male Infant ◽  
The Other ◽  
Review Of Literature ◽  
Harlequin Syndrome ◽  
Congenital Condition ◽  
Autonomic Disturbances

AbstractHarlequin syndrome is a condition characterized by autonomic dysfunction leading to hemifacial flushing on one side with pallor and impaired sweating on the other side. It is a rare condition that can be both congenital and acquired, with congenital cases being rarer, comprising ∼6% of all Harlequin syndrome cases. Harlequin syndrome is usually associated with other autonomic disturbances including Horner syndrome especially when presenting as a congenital condition. We reported the findings of a rare case of concomitant congenital Horner and Harlequin syndromes in an otherwise healthy 4-month-old male infant patient and provided a review of the current literature.

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