نتایج جستجو برای: aplasia cutis congenita

تعداد نتایج: 11513  

Journal: :Case Reports in Dermatology 2018

2010
Umar A. Qureshi Nisar Ahmed

Ann Saudi Med 30(2) March-April 2010 www.saudiannals.net 171 A two-hour-old female neonate, a product of nonconsanguineous marriage with unremarkable family history, was brought with well-defined bilaterally symmetrical and superficial erosions on the knees, trunk and lower limbs with sparing of scalp and mucosa (Figure 1). Biopsy revealed an absence of epidermis and superficial dermis. Antenat...

Journal: :Sri Lanka Journal of Child Health 2017

Journal: :Arquivos de Neuro-Psiquiatria 2008

Journal: :Skin health and disease 2023

Aplasia cutis congenita (ACC) is defined as complete or partial loss absence of skin at birth and it can occur on any part the body, but most commonly scalp. Single offspring with ACC have been reported in case reports, cases twins are rarely reported. Here, we report two ACC, monozygotic twin boys presented scattered over scalp vertex after birth. All lesions ulcers no hair healed scars, other...

2017
Virender Sekhon

Citation: Sekhon V. Aplasia Cutis Congenita of Scalp and Back: A Rare Entity. Ann Clin Case Rep. 2017; 2: 1367. ISSN: 2474-1655 Copyright © 2017 Sekhon V. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Case Report Published: 05 J...

Journal: :Dermatology online journal 2005
M R Vijayashankar

Aplasia cutis congenita is a rare anomaly presenting with absence of skin. The most common site is the scalp. No definite etiology is available. Heredity is proposed with not much evidence. We present an instance with ACC occurring in both mother and son, suggesting a hereditary etiology.

2017
Yasmin Florence Khodeja Islam Charles A. Williams Jennifer Jane Schoch Israel David Andrews

We present the case of a newborn with co-occurrence of Marfan syndrome and aplasia cutis congenita (ACC) and a family history significant for Marfan syndrome and ACC in the father. This case details a previously unreported mutation in Marfan syndrome and describes a novel coinheritance of Marfan syndrome and ACC.

Journal: :The Journal of the Association of Physicians of India 2014
Smita Ramachandran Kirtisudha Mishra Vineeta Vijay Batra

Aplasia cutis congenita is a rare developmental disorder of the skin of neonates, usually presenting as a solitary lesion over the scalp. We report an interesting presentation of AC along with the histopathological features in a neonate with extensive lesions over scalp as well as in bilaterally symmetrical areas over trunk and thighs; such symmetrical distributions being rarely reported.

Journal: :Indian pediatrics 1995
B C Bakane B Patil

Aplasia cutis congenita is a rare developmental anomaly that most commonly involves vertex of the scalp and may be associated with other congenital anomalies. Although isolated congenital absence of skin and congenital knee contracture is known,, association of these two conditions is not reported. We report on a child with absence of skin of left lower limb with contracture of left knee at birth.

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