12th congress of pediatric inherited metabolic disorders and endocrinology

12th congress of pediatric inherited metabolic disorders and endocrinology In date 2019-11-06 by _COMMA مركز تحقيقات رشد و تكامل كودكان _DAR _CITY Tehran was held. please refer to the following link to download all the papers of conference proceedings: _PROCEEDINGS 12th congress of pediatric inherited metabolic disorders and endocrinology

Accepted papers in 12th congress of pediatric inherited metabolic disorders and endocrinology

• Newly in diagnosis of type 1 diabetes mellitus

• Clinical, Laboratory Data & Outcome Of 7 Patients Affected Of Multiple Acyl-Coa Dehydrogenase Dehydrogenase

• Clinical, Laboratory, Molecular Data and Miglustat Outcome in 8 Iranian patients affected of Niemann Pick Type C

• Dyslipidemia and microbiota

• Efficacy of BCG vaccine for treatment of type1 diabetes

• A New Case of 3 –Hydroxyisobutyryl-CoA Hydrolase (HIBCH) Deficiency

• Niemann-Pick disease Type C

• A new treatment for 2-ketoglutaric aciduria: a case report

• Self-Care Education Effect on Patient Quality of Life with Phenyl Ketone Urea in Medical Center in Tehran, Iran

• Seizure pattern in Inborn Error of Metabolic Disorders

• How to diagnose and treat Tyrosinemia type 1

• Frequency of diabetic ketoacidosis in new cases of type 1 diabetes in children hospitalized in Pediatric Hospital from 2006 to 2019

• Transient and permanent hypothyroidism in Iran: what are the associated factors

• Early and Delayed puberty among Iranian children with obesity

• Organic Acidemia

• Metabolic Disorders, Genetic Abnormalities and Ophthalmology

• The Effects of Urtica Dioica on Diabetes

• Epidermal Nevus Syndrome AND Hypophosphatemic rickets

• New treatment strategies for lysosomal storage disorders

• Gaucher disease

• Diagnosis of a rare ciliopathy by genetic test -WHOLE EXOME SEQUENCING- in a nonconsanguineous marriage family: case report

• Obstructive Gastrointestinal Tract Disorders in cystic fibrosis

• Diagnosis of Primary Ciliary Dyskinesia by the identification of homozygote mutation in CCDC40 gene with whole-exome sequencing in a 12 years old patient: a case report

• How can we interpret metabolic tests

• غدد، معرفی یک مورد اختلال رشد و هیپوگلیسمی

• مقایسه دیابت بارداری وابسته به مصرف انسولین با دیابت بارداری وابسته به مصرف متفورمین و اثر آنها بر مارکرهای غربالگری سه ماهه اول بارداری در سال های 1387 تا 1398 در تهران

• دارو درمانی بیماران منتخب متابولیک؛ آیا درست انجام می دهیم

• غربالگری بیماری های متابولیک ارثی نوزادان

• Challenges of Family of Children with Phenylketonuria and its Impact on their Mental Health

• Clinical evaluation of the effect of restorative topical ointment on the process of open cutaneous wound healing on diabetic children: A double-blind randomized clinical triae

• خود مراقبتی در کودکان مبتلا به دیابت نوع 1

• چالش های پیش روی والدین کودکان مبتلا به اختلالات متابولیک

• بررسی ویژگی های روان سنجی ابزار اندازه گیری مدیریت خانواده ( FaMM ) و کاربرد آن در بررسی مدیریت خانواده در بیماری های مزمن دوره کودکی: مقاله مروری

• تعییین رضایتمندی والدین کودکان بستری در بخش غدد از مراقبت های پرستاری ارائه شده

• مروری بر عملکرد پرستاران در ارائه مراقبت های تسکینی در کودکان مبتلا به دیابت نوع 1

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