Type II vitamin D-dependent rickets with diabetic ketoacidosis. 2013

Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui

The high prevalence of vitamin D deficiency in relation to diabetes mellitus is well reported in the literature. However, type I diabetes mellitus (T1DM) in association with resistant rickets is extremely rare and reported in only one previous case. The authors describe here a case of type II vitamin D-dependent rickets (VDDR type II) in a 10-year-old Indian girl who presented with diabetic ketoacidosis (DKA). DKA as a presenting manifestation of T1DM in a patient with VDDR type II has never been reported before in worldwide literature.

UI MeSH Term Description Entries
D008310 Malocclusion Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982) Angle's Classification,Crossbite,Tooth Crowding,Cross Bite,Angle Classification,Angles Classification,Bite, Cross,Bites, Cross,Classification, Angle's,Cross Bites,Crossbites,Crowding, Tooth,Crowdings, Tooth,Malocclusions
D011859 Radiography Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film). Radiology, Diagnostic X-Ray,Roentgenography,X-Ray, Diagnostic,Diagnostic X-Ray,Diagnostic X-Ray Radiology,X-Ray Radiology, Diagnostic,Diagnostic X Ray,Diagnostic X Ray Radiology,Diagnostic X-Rays,Radiology, Diagnostic X Ray,X Ray Radiology, Diagnostic,X Ray, Diagnostic,X-Rays, Diagnostic
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003922 Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. Diabetes Mellitus, Brittle,Diabetes Mellitus, Insulin-Dependent,Diabetes Mellitus, Juvenile-Onset,Diabetes Mellitus, Ketosis-Prone,Diabetes Mellitus, Sudden-Onset,Diabetes, Autoimmune,IDDM,Autoimmune Diabetes,Diabetes Mellitus, Insulin-Dependent, 1,Diabetes Mellitus, Type I,Insulin-Dependent Diabetes Mellitus 1,Juvenile-Onset Diabetes,Type 1 Diabetes,Type 1 Diabetes Mellitus,Brittle Diabetes Mellitus,Diabetes Mellitus, Insulin Dependent,Diabetes Mellitus, Juvenile Onset,Diabetes Mellitus, Ketosis Prone,Diabetes Mellitus, Sudden Onset,Diabetes, Juvenile-Onset,Diabetes, Type 1,Insulin Dependent Diabetes Mellitus 1,Insulin-Dependent Diabetes Mellitus,Juvenile Onset Diabetes,Juvenile-Onset Diabetes Mellitus,Ketosis-Prone Diabetes Mellitus,Sudden-Onset Diabetes Mellitus
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000505 Alopecia Absence of hair from areas where it is normally present. Alopecia, Androgenetic,Baldness,Male Pattern Baldness,Pseudopelade,Alopecia Cicatrisata,Alopecia, Male Pattern,Androgenetic Alopecia,Androgenic Alopecia,Baldness, Male Pattern,Female Pattern Baldness,Hair Loss,Pattern Baldness,Alopecia Cicatrisatas,Alopecia, Androgenic,Alopecias, Androgenic,Androgenic Alopecias,Baldness, Female Pattern,Baldness, Pattern,Hair Losses,Loss, Hair,Losses, Hair,Male Pattern Alopecia
D016883 Diabetic Ketoacidosis A life-threatening complication of diabetes mellitus, primarily of TYPE 1 DIABETES MELLITUS with severe INSULIN deficiency and extreme HYPERGLYCEMIA. It is characterized by KETOSIS; DEHYDRATION; and depressed consciousness leading to COMA. Acidosis, Diabetic,DKA Diabetic Ketoacidosis,Diabetic Acidosis,Diabetic Ketosis,Ketoacidosis, Diabetic,Ketosis, Diabetic,Acidoses, Diabetic,DKA Diabetic Ketoacidoses,Diabetic Acidoses,Diabetic Ketoacidoses,Diabetic Ketoacidosis, DKA,Diabetic Ketoses,Ketoacidoses, Diabetic,Ketoacidosis, DKA Diabetic,Ketoses, Diabetic
D016916 Joint Deformities, Acquired Deformities acquired after birth as the result of injury or disease. The joint deformity is often associated with rheumatoid arthritis and leprosy. Acquired Joint Deformities,Acquired Joint Deformity,Deformities, Acquired Joint,Deformity, Acquired Joint,Joint Deformity, Acquired
D053098 Familial Hypophosphatemic Rickets A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported. Hypophosphatemic Rickets, X-Linked Dominant,Rickets, X-Linked Hypophosphatemic,Generalized Resistance To 1,25-Dihydroxyvitamin D,Hereditary Hypophosphatemic Rickets,Hereditary Vitamin D-Resistant Rickets,Hypocalcemic Vitamin D-Resistant Rickets,Hypophosphatemia, X-Linked,Hypophosphatemic Rickets, X-Linked Recessive,Rickets, Hereditary Vitamin D-Resistant,Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol,Vitamin D-Resistant Rickets, Hereditary,Vitamin D-Resistant Rickets, X-Linked,X-Linked Hypophosphatemia,Generalized Resistance To 1,25 Dihydroxyvitamin D,Hereditary Vitamin D Resistant Rickets,Hypocalcemic Vitamin D Resistant Rickets,Hypophosphatemia, X Linked,Hypophosphatemic Rickets, Familial,Hypophosphatemic Rickets, Hereditary,Hypophosphatemic Rickets, X Linked Dominant,Hypophosphatemic Rickets, X Linked Recessive,Hypophosphatemic Rickets, X-Linked,Rickets, Familial Hypophosphatemic,Rickets, Hereditary Hypophosphatemic,Rickets, Hereditary Vitamin D Resistant,Vitamin D Resistant Rickets With End Organ Unresponsiveness To 1,25 Dihydroxycholecalciferol,Vitamin D Resistant Rickets, Hereditary,Vitamin D Resistant Rickets, X Linked,X Linked Hypophosphatemia,X-Linked Hypophosphatemic Rickets

Related Publications

Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
April 1980, The New England journal of medicine,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
April 1996, Indian pediatrics,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
January 1980, Calcified tissue international,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
June 2006, Nihon rinsho. Japanese journal of clinical medicine,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
April 2007, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
August 1997, Acta paediatrica Japonica : Overseas edition,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
February 2014, Materia socio-medica,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
September 2005, The Journal of small animal practice,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
September 1988, Nihon Hifuka Gakkai zasshi. The Japanese journal of dermatology,
Sumantra Sarkar, and Rakesh Mondal, and Indira Banerjee, and Tapas Sabui
July 1991, European journal of pediatrics,
Copied contents to your clipboard!