congenital lamellar ichthyosis
Recently Published Documents


TOTAL DOCUMENTS

20
(FIVE YEARS 1)

H-INDEX

6
(FIVE YEARS 0)

2019 ◽  
Vol 12 (8) ◽  
pp. e228313
Author(s):  
Anja Saso ◽  
Benjamin Dowsing ◽  
Karen Forrest ◽  
Mary Glover

We report the case of a 3-week old girl in The Gambia who presented to hospital with an undiagnosed skin disorder evolving since birth. Using telemedicine to seek specialist dermatology advice abroad, she was diagnosed with and managed for suspected congenital lamellar ichthyosis. Poor early recognition and limited resources, for both acute and chronic care, created significant challenges to optimal management; these were overcome, in part, by adopting a common sense, back-to-basics approach to treatment and by empowering the parents to take ownership of their infant’s daily skin and eye care. This case highlights key global health issues associated with managing chronic, often debilitating, paediatric dermatological conditions in a low-income setting; namely, poor access to important diagnostic tools and medications, lack of experience and expertise in the management of severe skin disease and its associated complications, absence of long-term community support, alternative health beliefs and risk of sociocultural stigma.


2019 ◽  
Vol 58 (7) ◽  
pp. e135-e137 ◽  
Author(s):  
Anissa Zaouak ◽  
Ghaith Abdessalem ◽  
Rahma Mkaouar ◽  
Olfa Messaoud ◽  
Sonia Abdelhak ◽  
...  

2018 ◽  
Vol 66 (6) ◽  
pp. 856
Author(s):  
LindaMaria Genoveva De Piedade Sequeira ◽  
ShivanandC Bubanale ◽  
BhagyajyothiB Kurbet

2018 ◽  
Vol 10 (3) ◽  
pp. 166
Author(s):  
AndreaD Praticò ◽  
MariaElena Cucuzza ◽  
FlaviaLa Mendola ◽  
Angela D'Ambra ◽  
Pierluigi Smilari ◽  
...  

2015 ◽  
Vol 2 (15) ◽  
pp. 2343-2347
Author(s):  
Md. Jakeer Shaik ◽  
Rajesh Kumar Sethi ◽  
Lalat Barun Patra ◽  
Patra D P

2013 ◽  
Vol 59 (4) ◽  
pp. 28-32
Author(s):  
A O Emel'ianov ◽  
L S Sozaeva

A 16-year old boy, P.E., is described in whom the diagnosis of congenital lamellar ichthyosis was established at birth based on the clinical picture and confirmed by a molecular genetic study. Diabetes mellitus was first suspected at the age of 10 years based on the elevated fasting blood glucose (7.1 mmol/l) and HbA1c (7.4%) levels. The patient's medical history revealed that his maternal grandmother suffered diabetes mellitus and his mother had gestational diabetes during the second pregnancy. The patient presented with impaired carbohydrate tolerance in the absence of insulin resistance. The molecular genetic study of the GCK gene revealed a Gly80Ser mutation in the third exon sequence. We failed to find a report of the combination of congenital lamellar ichthyosis and type 2 MODY diabetes mellitus in the available literature.


Sign in / Sign up

Export Citation Format

Share Document